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Synthetic bone grafting material consisting of nanocrystalline hydroxyapatite (HA) embedded in a highly porous silica gel matrix, for active stimulation of collagen and bone formation. Because it is manufactured at 700ºC, Nanobone’s nanostructure is not sintered, allowing it to be completely remodelled over the course of time. Highly osteoconductive material, making it ideal for repairing defects around implants, filling sockets after extractions, ridge preservation techniques, sinus lifts, etc. Because it contains absolutely no animal products, the possibility of zoogenic infection or disease is ruled out. It comes in sterile vials, in two particle sizes: 0.6mm and 1.0mm, depending on the size of the defect to be repaired  Rapid bone formation. Full remodelling  Exceptional strength due to nanostructure. Synthetic and safe.

Nano Bone 1.2 ml 1.0 mm

to_fixed

Discount

<h5>Composition</h5>
Synthetic β-TCP
<h5>Porosity</h5>
80%
Pore Size: 300 – 500 microns
POROUS SYNTHETIC BONE BIOMATERIAL&nbsp;
adbone TCP is a totally synthetic bone graft material made of pure&nbsp;beta-tricalcium phosphate (β-TCP).

THREE-DIMENSIONAL REGENERATION OF THE BONE&nbsp;
adbone TCP features a multidirectional interconnected porosity that guides the three dimensional regeneration of bone. As bone healing process occurs, adbone TCP is resorbed and replaced by new bone.

HIGHEST DEGREE OF POROSITY&nbsp;
adbone TCP was designed to achieve the highest degree of porosity without compromising the mechanical resistance.
<h3>Porosity:</h3>
80%
<h3>Pore Size:</h3>
400μm
<h3>MECHANICAL RESISTANCE:</h3>
3,0 MPa
<h5>adbone TCP has been designed to imitate natural bone</h5>
<h3></h3>
<h3>Characteristics</h3>
- Easy to handle:&nbsp;adbone TCP can be easily mixed with patient’s blood or autologous bone marrow. The hydrophilic behavior of adbone TCP confers a high cohesivity of the particles
- Totally synthetic:&nbsp;adbone TCP does not contain animal or human tissues or derivatives
- Vascularization: The interconnected porosity of adbone TCP forms an ideal environment for vascularization
- Radiopaque: adbone TCP is radiopaque, allowing the&nbsp;monitorization&nbsp;of the graft osseointegration
<table><tbody><tr><th>REFERENCES</th><th>GEOMETRY</th><th>RANGE SIZE</th><th>QUANTITY</th></tr><tr><td>TCP010505G</td><td rowspan="2">Granules</td><td>0.1 – 0.5 mm</td><td rowspan="2">0.5g x 1 Unit</td></tr><tr><td>TCP050105G</td><td>0.5 – 1 mm</td></tr><tr><td>TCP010505P</td><td rowspan="2">Granules</td><td>0.1 – 0.5 mm</td><td rowspan="2">0.5g x 5 Unit</td></tr><tr><td>TCP050105P</td><td>0.5 – 1 mm</td></tr><tr><td>TCP010510G</td><td rowspan="3">Granules</td><td>0.1 – 0.5 mm</td><td rowspan="3">1g x 1 Unit</td></tr><tr><td>TCP050110G</td><td>0.5 – 1 mm</td></tr><tr><td>TCP010210G</td><td>1 – 2 mm</td></tr><tr><td>TCP010510P</td><td rowspan="3">Granules</td><td>0.1 – 0.5 mm</td><td rowspan="3">1g x 5 Unit</td></tr><tr><td>TCP050110P</td><td>0.5 – 1 mm</td></tr><tr><td>TCP010210P</td><td>1 – 2 mm</td></tr><tr><td colspan="4">Other references and geometries are available upon request.</td></tr></tbody></table>

Medbone Adbone TCP Granules

next-dental

Natural Bovine Bone Substitution Material
CompactBone®&nbsp;B. Is A Highly Reliable, Extremly Pure, Natural Bone Substitution Material Made From Bovine Bone. The Mineral Composition, Physical, Chemical, And Biological Properties, And Special Hydrophilic Surface Closely Resemble The Characteristics Of Human Bone. The Uniquely Safe High-Temperature Manufacturing Process Removes All Organic Components And Prevents Immune Responses. CompactBone B. Is 100% BSE-Free And Contains No Proteins.
&nbsp;
Properties
&nbsp;Grain Size : 0.5 - 1.0 mm
-No Inflammatory Immune System Reactions
-Interconnecting Pore System For Quick Revascularization
-Slow, Delayed Resorption With Controlled Integration Due To New Bone Growth
-Hydrophilic Surface, Optimal Cell And Platelet Adhesion
-Safe And Sterile
-Easy Handling
&nbsp;
Indications: Implantology, Periodontology, Oral And Maxillofacial Surgery
&nbsp;
-Sinus Lift
-Vertical Augmentation
-Horizontal Augmentation
-Extraction Socket
-Furacation Defect
-Intraossary Defect
-Perimplantary Defect

Dentegris CompactBone B

<h1>Bone Chips Graft (0.5-1mm)</h1>
Atident is a cancellous human-sourced graft produced from the femoral heads.&nbsp;As has been shown in all international studies carried out to date, it supports the rapid formation of new alveolar bone tissue by inducing osteoblasts (bone-forming cells) in the area of application.
<h1>PRODUCT FEATURES:</h1>
<table><tbody><tr><th>Texture Type</th><td>Human Origin Allograft Bone Tissue</td></tr><tr><th>Product Structure</th><td>Granular bone chips between 0.5-1 mm in cancellous structure</td></tr><tr><th>Sterilization</th><td>Lyophilized, Gamma Sterilization, Zero Virus Inactive</td></tr><tr><th>Packaging</th><td>Double-layer sterile packaging</td></tr><tr><th>Guarantee</th><td>It is fully insured against production-related complications.&nbsp;</td></tr></tbody></table>
<h3>100% DOMESTIC PRODUCTION FROM 100% TURKISH DONORS</h3>
Atigen-Cell, Turkey's leading cell and tissue center for many "firsts" and "only"s, Atident Allograft Bone Grafts are produced from the femoral heads of bones provided by donations from Turkish donors.&nbsp;It is produced from the bones of living donors instead of deceased patients.
<h3>PRODUCTION WITH THE “LYOPHYLIZATION” METHOD</h3>
Atident Allografts are produced in Atigencell's world-class advanced laboratories, with patented production techniques.&nbsp;It is the "first and only" Allograft of Turkey, produced with the "LYOPHYLIZATION" method, which is the most technological production level.
<h3>100% SAFE, 100% STERILE</h3>
"Sterility Safety Level" is at its maximum in the production of freeze-dried Atident Allografts.&nbsp;Bones are selected from healthy donors.&nbsp;Bones deemed suitable are subjected to health screening with the highest analysis in line with the procedures.&nbsp;Every step is processed with patented superior medical techniques at absolute safety levels.&nbsp;Finally, it is sterilized by gamma rays in packaging. 
<h3>EXTRA ASSURANCE WITH INSURANCE</h3>
Each Atident Allograft product, produced with superior production techniques, high sterilization and packaged with gamma irradiation, is 100% insured against any production-related complications.&nbsp;In this way, Atident maximizes the level of assurance.
 
<table><tbody><tr><th>Texture Type</th><td>Human Origin Allograft Bone Tissue</td></tr><tr><th>Product Structure</th><td>Granular bone chips between 0.5-1 mm in cancellous structure</td></tr><tr><th>Sterilization</th><td>Lyophilized, Gamma Sterilization, Zero Virus Inactive</td></tr><tr><th>Packaging</th><td>Double-layer sterile packaging</td></tr></tbody></table>

Atident Bone Chips Graft (0.5-1mm)

Description
Bone-D XB (Bovine Xenograft) is manufactured by sintering technology (High Temperature) of Medpark so it is very good property in term of strength, porosity, and safety (BSE Free).&nbsp;
Bone-D XB is combined biocompatible and safety-proven materials to maximize convenience and quality during the surgery.&nbsp;
Bone-D XB&nbsp;has similar structural characteristics with human bones. Due to its high porosity, Bone-D XB provides the most optimal environment for promoting osteoblast adhesion, blood vessel formation, and bone regeneration.&nbsp;
Key Properties:&nbsp;Grain Size : 0.5 - 1.0 mm&nbsp;
1) Excellent Pore Struture
- Manufactured by sintering technology of MedPark &gt; Securing strength / porosity / BSE Free
- Extensive internal area
- Maintenance of ideal volume
2) Easy Manipulation
- Faster absorption by blood and saline for its porosity
- Applicable to various indication such as Socket Preservation, Sinus Lift, Periodontal Defects and Ridge Augmentation
3) High Wettability
- Stimulating new bone formation with great hydration with blood
- Osteoblast in blood helps the new bone formation
Indications:
- Dental implant surgery
- Socket Preservation
- Periodonal Defects
- Sinus lift&nbsp;
- Ridge Augmentation
- GBR cases
 
<img src="https://www.bdh.co.th/images/editor/Medpark-Bone-D---XB-(Bovine-Xenograft)-6.jpg" alt="Medpark-Bone-D---XB-(Bovine-Xenograft" width="1400">
<img src="https://www.bdh.co.th/images/editor/Medpark-Bone-D---XB-(Bovine-Xenograft)-7.jpg" alt="Medpark-Bone-D---XB-(Bovine-Xenograft" width="1400">

Bone-D XB (Bovine Xenograft) is manufactured by sintering technology (High Temperature) of Medpark so it is very good property in term of strength, porosity, and safety (BSE Free). 



Medpark Bone D

<img src="https://static.wixstatic.com/media/8b9816_824881072d124faeb32ea04518c03ed1~mv2.png/v1/fill/w_164,h_58,al_c,q_85,usm_0.66_1.00_0.01,enc_auto/Novoss%20Front%20design%20-%20Copy.png" alt="Novoss Front design - Copy.png" style="margin: 0px; padding: 0px; outline: 0px; vertical-align: baseline; background: transparent; object-position: 50% 50%; filter: var(--filter-effect-svg-url); -webkit-mask-image: var(--mask-image,none); -webkit-mask-position: var(--mask-position,0); -webkit-mask-size: var(--mask-size,100% 100%); -webkit-mask-repeat: var(--mask-repeat,no-repeat); position: static; box-shadow: rgb(0, 0, 0) 0px 0px 0px; user-select: none; width: 164px; height: 58px; object-fit: cover;">
<h2>Porous synthetic ceramic designed for the filling of bone voids or defects.</h2>
<h2></h2>
• Novoss induces regeneration and bone growth:
– Stimulates the proliferation and differentiation of osteoblasts

• Composition:
– 75% Hydroxyapatite
– 25% Tricalcium Phosphate (β-TCP)

• Highly interconnected porosity with an excellent mechanical resistance

• Novoss is replaced by new bone tissue
– Biphasic resorption due to its composition
<h5>INDICATIONS</h5>
Novoss is intended to be used as a bone void augmentation material for bone defects that are not intrinsic to the stability of the bony structure:
• Fractures with bone defect
• Vertebral arthrodesis
• Tibial osteotomy
• Tibial and femoral fracture
• Total knee and hip revision
• Spine Surgery
<img src="https://static.wixstatic.com/media/8b9816_4858e06d2bbe4449b016d1473af0bbb7~mv2.jpg/v1/fill/w_418,h_170,al_c,q_80,usm_0.66_1.00_0.01,enc_auto/page%201%20-%20Copy.jpg" alt="page 1 - Copy.jpg" style="margin: 0px; padding: 0px; outline: 0px; vertical-align: baseline; background: transparent; object-position: 50% 50%; filter: var(--filter-effect-svg-url); -webkit-mask-image: var(--mask-image,none); -webkit-mask-position: var(--mask-position,0); -webkit-mask-size: var(--mask-size,100% 100%); -webkit-mask-repeat: var(--mask-repeat,no-repeat); position: static; box-shadow: rgb(0, 0, 0) 0px 0px 0px; user-select: none; width: 418px; height: 170px; object-fit: cover;">
<h6>Cellular Adhesion after 5 Days</h6>
<img src="https://static.wixstatic.com/media/8b9816_f11e989d0984447aa6d7cbd8f8001edd~mv2.png/v1/fill/w_265,h_230,al_c,q_85,usm_0.66_1.00_0.01,enc_auto/Porosity.png" alt="Porosity.png" style="margin: 0px; padding: 0px; outline: 0px; vertical-align: baseline; background: transparent; object-position: 50% 50%; filter: var(--filter-effect-svg-url); -webkit-mask-image: var(--mask-image,none); -webkit-mask-position: var(--mask-position,0); -webkit-mask-size: var(--mask-size,100% 100%); -webkit-mask-repeat: var(--mask-repeat,no-repeat); position: static; box-shadow: rgb(0, 0, 0) 0px 0px 0px; user-select: none; width: 265px; height: 230px; object-fit: cover;">
<img src="https://static.wixstatic.com/media/8b9816_5217ff6a608d4974bf10d5c61bc18a4e~mv2.png/v1/fill/w_266,h_230,al_c,q_85,usm_0.66_1.00_0.01,enc_auto/Pore%20Size.png" alt="Pore Size.png" style="margin: 0px; padding: 0px; outline: 0px; vertical-align: baseline; background: transparent; object-position: 50% 50%; filter: var(--filter-effect-svg-url); -webkit-mask-image: var(--mask-image,none); -webkit-mask-position: var(--mask-position,0); -webkit-mask-size: var(--mask-size,100% 100%); -webkit-mask-repeat: var(--mask-repeat,no-repeat); position: static; box-shadow: rgb(0, 0, 0) 0px 0px 0px; user-select: none; width: 266px; height: 230px; object-fit: cover;">
<img src="https://static.wixstatic.com/media/8b9816_2937b6e87280430eb532191561f07e1c~mv2.png/v1/fill/w_450,h_230,al_c,q_85,usm_0.66_1.00_0.01,enc_auto/Mechanical%20Resistence.png" alt="Mechanical Resistence.png" style="margin: 0px; padding: 0px; outline: 0px; vertical-align: baseline; background: transparent; object-position: 50% 50%; filter: var(--filter-effect-svg-url); -webkit-mask-image: var(--mask-image,none); -webkit-mask-position: var(--mask-position,0); -webkit-mask-size: var(--mask-size,100% 100%); -webkit-mask-repeat: var(--mask-repeat,no-repeat); position: static; box-shadow: rgb(0, 0, 0) 0px 0px 0px; user-select: none; width: 450px; height: 230px; object-fit: cover;">
<img src="https://static.wixstatic.com/media/8b9816_da9bfeac86954e8f84502e69802341fa~mv2.jpg/v1/fill/w_529,h_456,al_c,q_80,usm_0.66_1.00_0.01,enc_auto/page%202%20-%20Copy.jpg" alt="page 2 - Copy.jpg" style="margin: 0px; padding: 0px; outline: 0px; vertical-align: baseline; background: transparent; object-position: 50% 50%; filter: var(--filter-effect-svg-url); -webkit-mask-image: var(--mask-image,none); -webkit-mask-position: var(--mask-position,0); -webkit-mask-size: var(--mask-size,100% 100%); -webkit-mask-repeat: var(--mask-repeat,no-repeat); width: 529px; height: 456px; object-fit: cover;">
<h5>EASY HANDLING</h5>
<img src="https://static.wixstatic.com/media/8b9816_f92bbba86dcf4598b62ca3bb53cfa9d5~mv2.jpg/v1/fill/w_430,h_274,al_c,q_80,usm_0.66_1.00_0.01,enc_auto/page%202%20-%20Copy%20(2).jpg" alt="page 2 - Copy (2).jpg">

Porous synthetic ceramic designed for the filling of bone voids or defects.• Composition: – 75% Hydroxyapatite – 25% Tricalcium Phosphate (β-TCP)


Mediprex NovoOSS

Teebone is an osteoconductive alloplastic material designed for bone substitution. Its biphasic nature allows a controlled resorption profile similar to human bone. Due to its composition, 75% Hydroxiapatite and 25% Beta tricalcium phosphate, Teebone regenerates new bone through two different stages of activation. The breakdown of B-TCP by the osteoclast will free ions that enhance bone grow, while the hydroxyapatite acts as support for the bone ingrown whiting the graft, being slowly substituted.
<h6>Indications</h6>
<img src="https://static.wixstatic.com/media/8b9816_21a5798d82fa4ca8b3f92f3d913d1d1e~mv2.jpg/v1/fill/w_630,h_185,al_c,q_80,usm_0.66_1.00_0.01,enc_auto/tc1%20-%20Copy.jpg" alt="tc1 - Copy.jpg" style="height: undefined;width: undefined"/>
<h5>Key Features &amp; Benefits</h5>
<img src="https://static.wixstatic.com/media/8b9816_0cd53ff55d3846af972713580ff24073~mv2.png/v1/fill/w_153,h_100,al_c,q_85,usm_0.66_1.00_0.01,enc_auto/1_2.png" alt="1.2.png" style="height: undefined;width: undefined"/>
<h6>No Membrane</h6>
It is not necessary to use membrane, due to its physical and mechanical properties.
<img src="https://static.wixstatic.com/media/8b9816_bad74339cc9743ffbc7bfccfa7ed0577~mv2.png/v1/crop/x_0,y_0,w_494,h_326/fill/w_151,h_100,al_c,q_85,usm_0.66_1.00_0.01,enc_auto/1_5.png" alt="1.5.png" style="height: undefined;width: undefined"/>
<h6>Security</h6>
100% synthetic and 100% resorbable
<img src="https://static.wixstatic.com/media/8b9816_54e80512c9f146d6aaf23c377410450f~mv2.png/v1/crop/x_0,y_0,w_491,h_326/fill/w_150,h_100,al_c,q_85,usm_0.66_1.00_0.01,enc_auto/1_4.png" alt="1.4.png" style="height: undefined;width: undefined"/>
<h6>Easy Handling</h6>
teebone® is very hydrophilic which confers an excellent cohesivity between the particles.
<img src="https://static.wixstatic.com/media/8b9816_18f288c0076546dab93854a2042f5b80~mv2.png/v1/fill/w_154,h_94,al_c,q_85,usm_0.66_1.00_0.01,enc_auto/1_6.png" alt="1.6.png" style="height: undefined;width: undefined"/>
<h6>Vascularisation</h6>
teebone® induces a remarkable vascularisation.
<img src="https://static.wixstatic.com/media/8b9816_4ae19c09c2b942bfaa39d99774e60122~mv2.png/v1/fill/w_154,h_100,al_c,q_85,usm_0.66_1.00_0.01,enc_auto/1_3.png" alt="1.3.png" style="height: undefined;width: undefined"/>
<h6>Total Resorption</h6>
teebone® is replaced by new vital bone within 6 -24 months.
<img src="https://static.wixstatic.com/media/8b9816_64ce0e79a2d7401c81630fc005ddc8fb~mv2.png/v1/fill/w_154,h_94,al_c,q_85,usm_0.66_1.00_0.01,enc_auto/1_7.png" alt="1.7.png" style="height: undefined;width: undefined"/>
<h6>Radiopaques</h6>
Allows the perfect monitorization of osteointegration.
<img src="https://static.wixstatic.com/media/8b9816_e8cfc96b1e9345c3a9922df2b3525440~mv2.jpg/v1/fill/w_979,h_290,al_c,q_80,usm_0.66_1.00_0.01,enc_auto/tc2%20-%20Copy.jpg" alt="tc2 - Copy.jpg" style="height: undefined;width: undefined"/>

<h5>Device Description</h5>
teebone® BCP is a synthetic macroporous ceramic, containing hydroxyapatite and beta tricalcium phosphate, that does not incorporate a medical substance, nor tissues or blood products. The porous synthetic ceramic, containing beta tricalcium phosphate has been widely studied in the market and is not new. teebone® BCP is a sterile, single use, product that is gamma ray radiated using 25kGy. The macroporous ceramic allows an excellent osseointegration, as well as a total vascularization of the implant due to the interconnected porosity. teebone® BCP is designed for the filling of bone voids or defects of the skeletal system, replacing the bone structure gap. Due to the interconnected porosity of teebone® BCP, the implant can be total vascularized which allows an excellent osseointegration. New bone formation will occur and slowly replace the porosity of the implant, and the implant itself.
<h5>Intended Use</h5>
teebone® BCP, is a porous synthetic ceramic, designed for the filling of bone voids or defects of the skeletal system that are not intrinsic to the stability of the bony structure.
<h5>Mechanism of Action</h5>
According to the size and geometry of the bone defect, the surgeon establishes the appropriate dosage form to be applied. Irregular bone defects can be filled with granules or combinations of granules, blocks and cylinders.
Bone defects with defined geometric shape can be filled with blocks and cylinders.
Before implantation, teebone® BCP should be impregnated with patient’s blood or autologous bone marrow, in order to introduce blood cells, growth factors and, in case of bone marrow , osseoprogenitor cells into the graft.
After the impregnation step, the device should be immediately placed into the bone defect, in contact with cancellous tissue. The bone surface must be freshened and slightly bleeding to ensure an appropriate supply of blood cells and growth factors to the entire graft material.
The filling of the bone defect must be completed with a slight impaction and the wound closure must be complete and airtight.
The combination of teebone® BCP with any medical substance during implantation is carried out under the surgeon’s responsibility.
<h5>Precautions</h5>
As with any surgical procedure, care should be exercised in treating individuals with preexisting conditions that may affect the success of the surgical procedure. This includes individuals with bleeding disorders of any etiology, long-term steroidal therapy, immunosuppressive therapy, or high dosage radiation therapy.
Avoid overfilling the bone defect site or attempt to pressurize the treatment site.
teebone® BCP  should not be used at infected sites.
teebone® BCP is not intended for load-bearing uses. It is important to ensure that the area where the teebone® BCP have been implanted be properly secured mechanically with rigid fixations to strengthen the surroundings.
Attempts should not be made to modify the size of the granules or to change their shape. Experienced users may, if required adapt the cylinders or blocks to the defect by careful mechanical reworking prior to implantation, without compromising their function (e.g. pronounced comminution, cutting). Machining the cylinders or block should be performed with them hydrated (e.g. blood or saline solution), and NOT performed in situ to prevent ceramic dust entering the wound bed, which would induce macrophage activity in the form of inflammatory reaction. The dust resulting from this procedure must be carefully removed before inserting the implant.
teebone® BCP must be properly secured to prevent potential migration and should only be used in surgical procedures where bone grafts substitutes are adequately contained. 
<h5>Composition</h5>
teebone® BCP consists of 75% of  hydroxyapatite and 25% of β-TCP and comply with ISO 13779-1:2008 – Implants for surgery – Hydroxyapatite – Part 1: Ceramic hydroxyapatite.
Table – teebone® BCP composition.
<h5>Compound</h5>
<h5>Synonyms</h5>
<h5>Formula</h5>
<h5>CAS Number</h5>
<h5>Supplier</h5>
Beta-Tricalcium Phosphate
Hydroxyapatite
Tricalcium diphosphate
Calcium hydroxyapatite
β-Ca3(PO4)2
Ca5(PO4)3(OH)
7758-87-4
12167-74-7
Himed
Himed
<h5>Control of Raw Materials</h5>
All lots of raw materials used in the production of teebone® BCP are fully traceable. The control of raw material is performed according to the following processes:
<ol>
<li>Incoming Inspection</li>
</ol>
<ul>
<li>All received raw materials and production materials are identified inspected and labeled by qualified personnel according to applicable procedures.</li>
<li>The CoC and/or CoA and/or MDS documents, which are obligatory provided by the suppliers are verified and properly maintained.</li>
<li>The incoming inspection results are documented, and the records are filed as quality records.</li>
<li>The materials are issued for use in the process only after this inspection and approval.</li>
</ul>
   2.Traceability
<ul>
<li>The Company maintains traceability of all lots of raw materials used.</li>
<li>All materials and products in all manufacturing process stages are identified and labeled</li>
<li>The identification of the products, together with the data and information collected on manufacturing inspection and testing enable full traceability on the product.</li>
<li>The Company maintains traceability of lots of products manufactured.</li>
<li>This system ensures full information concerning products in case of non-conformities, complaints, returned products or any other reason.</li>
</ul>
<h5>Sterilization Method</h5>
teebone® BCP is sterilized by gamma radiation at Synergy Helath, now part of STERIS, at the Reading Facility site (Marcus Close Reading Berkshire RG30 4EA United Kingdom). The Synergy Health firm is certified by the means of the system ISO 9001 / EN ISO 13485 by the BSI certifying body firm and is registered FDA facility nº 3002807310.
<h5>Sterilization Validation</h5>
The sterilization method was validated according to EN ISO 11137-1:2006 “Sterilization of health care products – Radiation – Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices”, EN ISO 11137-2:2013 “Sterilization of health care products – Radiation – Part 2 : Establishing the sterilization dose, EN ISO 11737-1:2006 “Sterilization of medical devices – Microbiological methods – Part 1: Determination of a population of microorganisms on products” and EN ISO 11737-2:2009 “Sterilization of medical devices – Microbiological methods – Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process”.
The validation of the sterilization method of teebone® BCP included: maximum dose compatibility test, VDmax method and dose mapping.
<h5>Packaging Validation</h5>
In the packaging system of granules, the sterile barrier is constituted by the pouch. The sterile barrier of the packaging system of the preform shapes is constituted by the blister.
<h5>Biocompatibility</h5>
The use of hydroxyapatite and β-Tricalcium phosphate in vivo is well known and has been studied and evaluated in numerous animal and human studies over the years. Furthermore, teebone® BCP has been manufactured and distributed in the European market for 7 years without any adverse event to report up to date. The performance of teebone® BCP in the areas of intended uses, have proven that the material is non-toxic, biocompatible, resorbable and gradually replaced by new bone while in contact with vital bone.
<h6>(Expiry Date: 30/09/2023)</h6>

Medibrex Teebone Biphasic Bone Graft

Colla-DM is purified bovine collagen type I derived from bovine of BSE free zone authorized by OIE.&nbsp;
Product Features:
1) Adhesive property & Flexibility
- Easy manipulation and placement
- High hydrophilic property and excellent flexibility
2) Multiple-Layered Structure
- Effective bone & tissue regeneration by securing enough space maintenance
- Facilitating proliferation of osteoblasts
3) Safety:
- Derived from bovine of BSE (Bovine Spongiform Encephalopathy) Free zone authorized by OIE (Office International Des Epizooties)
Resorbtion Period: 3-6 months
Indications: Sinus Lift / Ridge augmentation / Fenestration defects / Horizontal augmentation / Alveolar ridge reconstruction / Dehiscence
 
Resorbable collagen membrane having both&nbsp;advantages of soft and hard type
<img src="https://www.bdh.co.th/images/editor/Colla-DM-%E0%B8%9A%E0%B8%97%E0%B8%84%E0%B8%A7%E0%B8%B2%E0%B8%A1.jpg" alt="Medpark Colla-DM Resorbable Collagen Membrane Implant Brand Bone Graft Brand Bone Graft for Implant regenerative materials and dentistry Best Bone Graft วัสดุปลูกกระดูกสำหรับงานรากเทียม / วัสดุปลูกกระดูกคุณภาพสูง / แนะนำวัสดุปลูกกระดูก / แนะนำ Bone graft / ผู้แทนจำหน่าย Bone Graft / Bone Graft ในประเทศไทย /BDH Medical Supply /บีดีเอชเมดิคอล ซัพพลาย / bone graft dealer / บริษัทรากเทียม ">
<table><tbody><tr><td>Adhesive Property & Flexibility</td><td>· Easy manipulation and placement
· High hydrophilic property and excellent flexibility</td></tr><tr><td>Multiple-Layered Structure</td><td>· Effective bone & tissue regeneration&nbsp;by securing enough space maintenance
· Facilitating proliferation of osteoblasts</td></tr><tr><td>Safety</td><td>· Using purified bovine collagen type I
· Derived from bovine of BSE free zone authorized by OIE</td></tr></tbody></table>

Colla-DM is purified bovine collagen type I derived from bovine of BSE free zone authorized by OIE. 

Product Features:

1) Adhesive property & Flexibility

- Easy manipulation and placement

- High hydrophilic property and excellent flexibility

Medpark Colla-D  (Resorbable Collagen Membrane)

Assuming that the clinical requirements for a barrier membrane are satisfied, individual preferences for the handling properties play a major role in the choice of collagen membranes. The easy handling of naturesQue&nbsp;ColTect P&nbsp;enables diverse applications in therapeutic concepts that include the use of regenerative measures.
<h4>Structure, design, and stability</h4>
<figure><a href="https://www.bego.com/fileadmin/user_upload/Images_Contents/Implants/Biomaterialien/naturesQues/BIS_naturesQues_ColTect-P_5_Membran_300x_gekippt-45.jpg" class="lightbox" rel="lightbox[4195]"><img class="image-embed-item" src="https://www.bego.com/fileadmin/_processed_/d/2/csm_BIS_naturesQues_ColTect-P_5_Membran_300x_gekippt-45_35c4c02e98.jpg" width="320" height="213" style="width: auto; display: block;"></a><figcaption>Scanning electron microscopy image of
naturesQue&nbsp;ColTect P.</figcaption></figure>
naturesQue&nbsp;ColTect P&nbsp;is manufactured from purified collagen-rich tissue. Using a gentle method, the collagen is minimally crosslinked to give the membrane a predictable resorption profile with maximum tissue tolerability. A crosslinked structure prevents premature enzymatic cleavage of the collagen fibers and gives
naturesQue&nbsp;ColTect P&nbsp;a reproducible and reliable barrier function that is adapted to the time profile of bone healing.
This produces a highly versatile and strong membrane with comfortable handling properties.
naturesQue&nbsp;ColTect P&nbsp;is made up of a layer of intact collagen fibers. The membrane is not side specific.
<h4>Requirements profile for a collagen membrane</h4>
Collagen membranes alone do not have sufficient mechanical stability to shape and protect defect contours. For this reason naturesQue&nbsp;ColTect P&nbsp;is used together with bone substitute materials such as naturesQue&nbsp;SemOss B&nbsp;or naturesQue&nbsp;MaxOss P.
The use of bone substitute materials creates a volumizing framework in the defect space that is used by the osteoblasts as a substrate for bone deposition.
A barrier membrane protects the spaces in the bone defect and prevents the ingrowth of soft tissues. The job of the membrane is to establish and maintain a barrier that is permeable to nutrients between the bone and soft tissue. The membrane also stabilizes the augmentation material by covering the bone defect. The barrier function of naturesQue&nbsp;ColTect P&nbsp;lasts about 3 months, which is sufficiently long to ensure adequate bone healing.
<figure><a href="https://www.bego.com/fileadmin/user_upload/Images_Contents/Implants/Biomaterialien/naturesQues/BIS_naturesQues_ColTect_P_pur_flex_forceps.jpg" class="lightbox" rel="lightbox[4195]"><img class="image-embed-item" src="https://www.bego.com/fileadmin/_processed_/0/0/csm_BIS_naturesQues_ColTect_P_pur_flex_forceps_41c38bcfa8.jpg" width="320" height="213" style="width: auto; display: block;"></a></figure>
<figure><a href="https://www.bego.com/fileadmin/user_upload/Images_Contents/Implants/Biomaterialien/naturesQues/BIS_naturesQues_ColTect-P_PosteriorFigureC_HiRes_V2.jpg" class="lightbox" rel="lightbox[4195]"><img class="image-embed-item" src="https://www.bego.com/fileadmin/_processed_/6/a/csm_BIS_naturesQues_ColTect-P_PosteriorFigureC_HiRes_V2_9cc44828f8.jpg" width="320" height="213" style="width: auto; display: block;"></a></figure>
<figure><a href="https://www.bego.com/fileadmin/user_upload/Images_Contents/Implants/Biomaterialien/naturesQues/BIS_naturesQues_ColTect_P_pur_forceps_01.jpg" class="lightbox" rel="lightbox[4195]"><img class="image-embed-item" src="https://www.bego.com/fileadmin/_processed_/4/c/csm_BIS_naturesQues_ColTect_P_pur_forceps_01_d6c7940d97.jpg" width="320" height="213" style="width: auto; display: block;"></a></figure>
<h4>Handling and feel</h4>
<figure><a href="https://www.bego.com/fileadmin/user_upload/Images_Contents/Implants/Biomaterialien/naturesQues/BIS_naturesQues_ColTect-P_Hand-Hapt_1.png" class="lightbox" rel="lightbox[4195]"><img class="image-embed-item" src="https://www.bego.com/fileadmin/_processed_/f/2/csm_BIS_naturesQues_ColTect-P_Hand-Hapt_1_a1d5b1f9f2.png" width="200" height="141" style="width: auto; display: block;"></a></figure>
<figure><a href="https://www.bego.com/fileadmin/user_upload/Images_Contents/Implants/Biomaterialien/naturesQues/BIS_naturesQues_ColTect-P_Hand-Hapt_2.png" class="lightbox" rel="lightbox[4195]"><img class="image-embed-item" src="https://www.bego.com/fileadmin/_processed_/5/f/csm_BIS_naturesQues_ColTect-P_Hand-Hapt_2_61facd2fc2.png" width="200" height="141" style="width: auto; display: block;"></a></figure>
The naturesQue&nbsp;ColTect P&nbsp;membrane can be applied wet or dry. The membrane is cut to size so that the piece overlaps the margin of the defect by about 2 mm. When dry, naturesQue&nbsp;ColTect P&nbsp;is a sturdy, stable membrane. Wetting the membrane with saline or blood makes naturesQue&nbsp;ColTect P&nbsp;flexible, enabling it to be adapted to the defect contours.
It is not usually necessary to fix naturesQue&nbsp;ColTect P&nbsp;because the membrane can be easily wetted and adheres to the bone walls. Nevertheless, naturesQue&nbsp;ColTect P&nbsp;can be repositioned should this be necessary. If needed, naturesQue&nbsp;ColTect P&nbsp;can be sutured or fixed with pins.
<h4>naturesQue&nbsp;ColTect P&nbsp;put into context</h4>
Origin
<ul><li>Porcine peritoneum</li></ul>
Composition
<ul><li>Intact collagen fibers</li><li>Stabilized by reliable minimal crosslinking</li></ul>
Processing
<ul><li>Collagen-rich peritoneum</li><li>Cleaning and removal of non-collagenous proteins</li><li>Stabilization of the collagen fibers using minimal crosslinking</li><li>Washing, rinsing, and drying</li><li>Measurement, packaging, and sterilization</li><li>Quality Control</li></ul>
Application
<ul><li>Remove with sterile instruments</li><li>Processed wet or dry</li><li>Adapt to the size of the defect, overlapping by about 2 mm</li><li>Closed healing is recommended</li><li>No specific side for positioning</li><li>Can be repositioned</li></ul>
Consistency/Feel
<ul><li>Dry: Stable and rigid, sturdy</li><li>Wet: Can be draped, sturdy, adhesive, not sticky</li><li>Does not stretch</li><li>Tear resistant</li></ul>
Resorption
<ul><li>Resorption time between 12 and 16 weeks</li></ul>

Assuming that the clinical requirements for a barrier membrane are satisfied, individual preferences for the handling properties play a major role in the choice of collagen membranes. The easy handling of naturesQue ColTect P enables diverse applications 

Bego NaturesQue ColTect P ( Xenogeneic porcine barrier membrane )

MedPark BOSS is a xenograft material using bovine cancellous bone blister completely auto the space where new bone tissue is formed by filling defects or bony voids of the oral and maxillofacial region due to a surgical injury or a non-surgical injury. 1. Deliver a double-packed product to the operating room while keeping it sterilized. 2. Do not use BOSS if the sterile package is damaged or opened. 3. Do not use it if any foreign materials are found inside the vial. 4. Do not use a BOSS bone graft after the expiration date. The validity period is 3(three) years from the date of manufacture. 5. Read and fully understand 'Directions for Use' before surgery and be sure that they know exactly how to use BOSS. 6. The surgical instruments must be sterilized before the operation.
7. BOSS is an implantable medical device that should be used in a clean environment and operating room. The general principles of sterile handling and patient medication must be followed when using BOSS.
1. When using it, peel off the mucoperiosteal to Tyvek film. Hold to ing BOSS vial firmly, and remove the cap. Dispense the granules of BOSS into a sterile container.
2. After exposure to the bony defect with mucoperiosteal and flap, completely remove the transgranulartissue and mucoperiosteal tissue.
3. When opening the sterile package, never store remained product after.
4. After wetting the BOSS granules, fill up the defect area with the bone graft.
5. Xenograft materials can be mixed with autogenous bone at the discretion of a clinician.
6. After wetting, the and of BOSS in saline solution, remove any excess fluid, and granulation is filled into the bone defect. The graft material should be treated carefully neither to damage nor to change the transplant material.
7. After filling the graft, cover the surgical site with types,p, and should be fixed by sutures. Be sure to completely seal the implantation site to prevent exposure.
fundamentally, the use of powder type is recommended for small defects (up to 2 dental alveoli) and for augmenting autogenous grafts. The chip type is recommended for large defects (&gt; 2 dental alveoli, sinus lifts), however, preferences can vary from dentist to dentist. Powder and Chip expiratiosecure package nicotinism and can be mixed at the dentist's discretion. This product is supplied in a sterile container. Store as it is at room temperature(1℃ to 30℃) in the shade before use. The product must not be used if the sterile packaging is damaged or opened. The contents of the blister package or vial are designed for single use only. Discard any unused material after opening. The expiration date is 3the years from the date of manufacture. Do not use and re-sterilize products that have expired.1. Warnings
1) Discard any unused material after opening. Never reuse! 2) Do not use to and patients with opened or damaged or if the expiration date has been exceeded. 3) This product should only be used by trained dentists or oral surgeons.
2. Patients with the following diseases are prohibited.
1) Patients with osteomyelitis 2) Patients with severe liver dysfunction 3) Patients with severe cardiac dysfunction.
3. Side Effect
Incompatibility reactions with MedPark BOSS cannot be excluded. Possible complications which may occur with any surgery include swelling at the surgical site, flap sloughing, bleeding, local inflammation, bone loss, infection, or pain.
4. General precautions
1) In general, the conditions considered as standard contraindications for bone graft are metabolic diseases, osteoporosis, steroid therapy, and inflammatory the inflammatory and inflammatory autoinflammatory an inflammatory auto completely auto immunautoimmune e diseasesifnicotinis. 2) For bone regeneration, the product is only implantable to bone tissue that is directly connected to living bone tissue and host bone. In the case of large injuries, the addition of autogenous cancellous bone or bone marrow can improve the regeneration process. Experience has shown that movement due to increased physical loads (compression loads) or implantation of implants (2-step procedures) should be avoided until several weeks after insertion of the product. Experiments have shown that the physical loading (compression load) of this product'sskeletally immature and augmented areas is possible after 6 months at the earliest. Implant placement time is determined by the amount of remaining local bone.
5. Pregnant and lactating women, infants, children 1) Do not use BOSS for pregnant or lactating women. 2) It should not be used in Using the amount corresponding to the defect within the maximum allowable dosage recommended and. (&lt;18 years of age of no radiographic evidence of epiphyseal closure)
6. Application notes 1) Do not leave any parenchyma or other soft tissue on the defective area to be implanted. 2) This product has a low mechanical strength, so be careful when filling the contents. 3) Do not overfill defective or surgical sites. 4) The defect site and the surgical site must be completely closed. 7. Others 1) One patient can be implanted with a maximum of 2.5 g BOSS during one procedure and their lifespan. 2) Using the amount corresponding to the defect within the maximum allowable dosage is recommended. The amount of the product can be determined at the discretion of the dentist. Specifications type: chip model name: MBXB-C120-100 Saiz: 1.0 g - 2.0 contents: 1.0 g

MedPark BOSS

B Dent

Miller Root Elevator&nbsp;
2 pcs . (Right & Left)
Made in&nbsp;Pakistan

Pakistan Miller Root Elevator Right & Left (2pcs)

Crossbar Root Elevator
2 pcs (Right & Left)&nbsp;Used in oral surgery to loosen a tooth from its socket for extraction purposes. They assist in severing the PDL ligament of the tooth for easy extraction.

 Used in oral surgery to loosen a tooth from its socket for extraction purposes. They assist in severing the PDL ligament of the tooth for easy extraction.​