Biongraft Bone Cement Applicator Guide Wire (Kirschner wire)
- Risk class
- Class IIa
- CND nomenclatures code
- P099002
- Trade name
- Biongraft
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- 08681781334472
- Basic UDI
- B-08681781334472
- Version date
- February 05, 2024
- Manufacturer last update
- November 01, 2021
- Active status
- No
- Manufacturer name
- Bonegraft Biomaterials Co.
- Country
- Turkey
- Country type
- EU_EXTENDED
- Address
- 7410 Sk. Kemalpaşa Mh. İzmir
- info@bonegraft.com.tr
- Competent authority
- Turkish Medicine and Medical Devices Agency
- Applicable legislation
- MDD (Directive 93/42/EEC on Medical Devices)
- Placed on the market
- Turkey
- Market available
- Austria:None~None, Belgium:None~None, Bulgaria:None~None, Croatia:None~None, Cyprus:None~None, Czechia:None~None, Denmark:None~None, Estonia:None~None, Finland:None~None, France:None~None, Germany:None~None, Greece:None~None, Hungary:None~None, Iceland:None~None, Ireland:None~None, Italy:None~None, Latvia:None~None, Liechtenstein:None~None, Lithuania:None~None, Luxembourg:None~None, Malta:None~None, Netherlands:None~None, Norway:None~None, Poland:None~None, Portugal:None~None, Romania:None~None, Slovakia:None~None, Slovenia:None~None, Spain:None~None, Sweden:None~None, Turkey:None~None, United Kingdom (Northern Ireland only):None~None
- Human tissues
- No
- Animal tissues
- No
ORTHOPAEDIC CEMENT PREPARATION AND APPLICATION DEVICES AND KITS
Access comprehensive regulatory information for Biongraft Bone Cement Applicator Guide Wire (Kirschner wire) in the European Union medical device market through Pure Global AI's free database. This Class IIa device is registered with EU EUDAMED under Primary DI 08681781334472 and manufactured by Bonegraft Biomaterials Co. in Turkey.
This page provides complete registration details including trade name (Biongraft), manufacturer information, competent authority (Turkish Medicine and Medical Devices Agency), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.