Sterilization Container Systems
- Risk class
- Class I
- CND nomenclatures code
- S010499
- Implantable
- No
- Reusable
- Yes
- Measuring function
- No
- Primary DI
- 08698913344223
- Basic UDI
- 8698913CON00152
- Version date
- December 18, 2024
- Manufacturer last update
- June 14, 2022
- Active status
- No
- Manufacturer name
- BAHADIR TIBBİ ALET CİHAZ VE İNŞAAT MAKİNA SAN. VE TİC. AŞ.
- Country
- Türkiye
- Country type
- EU_EXTENDED
- Address
- 29/1 Şabanoğlu OSB Mah. Vali M. Erdoğan Cebeci Bul. SAMSUN
- info@bahadir.com.tr
- Competent authority
- Turkish Medicine and Medical Devices Agency
- Applicable legislation
- MDR (REGULATION (EU) 2017/745 on medical devices)
- Placed on the market
- Türkiye
- 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, Türkiye:None~None, United Kingdom (Northern Ireland only):None~None
- Human tissues
- No
- Animal tissues
- No
STERILISATION CONTAINERS - OTHER
Access comprehensive regulatory information for Sterilization Container Systems in the European Union medical device market through Pure Global AI's free database. This Class I device is registered with EU EUDAMED under Primary DI 08698913344223 and manufactured by BAHADIR TIBBİ ALET CİHAZ VE İNŞAAT MAKİNA SAN. VE TİC. AŞ. in Türkiye.
This page provides complete registration details including 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.