INTRAMEDULLARY COMPRESSION NAIL (ICN) HUMERUS Ø8X295 mm (TI)
- Risk class
- Class IIb
- CND nomenclatures code
- P09120201
- Trade name
- GOLD ORTOPEDİ SANAYİ VE TİCARET LİMİTED ŞİRKETİ
- Implantable
- Yes
- Reusable
- No
- Measuring function
- No
- Primary DI
- D-86809415500429N
- Basic UDI
- B-86809415500429N
- Version date
- June 01, 2023
- Manufacturer last update
- November 12, 2021
- Active status
- No
- Manufacturer name
- GOLD ORTOPEDİ SANAYİ VE TİCARET LİMİTED ŞİRKETİ
- Country
- Turkey
- Country type
- EU_EXTENDED
- Address
- 03070 CAD. AYDINLAR MAH. 27580 Gaziantep
- ubb@zimed.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
INTRAMEDULLARY NAILS
Access comprehensive regulatory information for INTRAMEDULLARY COMPRESSION NAIL (ICN) HUMERUS Ø8X295 mm (TI) in the European Union medical device market through Pure Global AI's free database. This Class IIb device is registered with EU EUDAMED under Primary DI D-86809415500429N and manufactured by GOLD ORTOPEDİ SANAYİ VE TİCARET LİMİTED ŞİRKETİ in Turkey.
This page provides complete registration details including trade name (GOLD ORTOPEDİ SANAYİ VE TİCARET LİMİTED ŞİRKETİ), 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.