STERILIZATION CONTAINER SYSTEMS
- Risk class
- Class I
- CND nomenclatures code
- S010401
- Trade name
- CEYLAN
- Implantable
- No
- Reusable
- Yes
- Measuring function
- No
- Primary DI
- 08681092602321
- Basic UDI
- 86810926CEYLAN13730K4
- Version date
- April 06, 2024
- Manufacturer last update
- December 14, 2023
- Active status
- No
- Manufacturer name
- FATMA CEYLAN- CEYLAN MEDİKAL İMALAT İTHALAT İHRACAT DIŞ TİCARET
- Country
- Turkey
- Country type
- EU_EXTENDED
- Address
- Organize Sanayi Bölgesi Mh. 5. Cd. No:6/4 KAVAK SAMSUN 55040 samsun
- ceylantr@ceylantibbi.com.tr
- Competent authority
- Turkish Medicine and Medical Devices Agency
- Applicable legislation
- MDR (REGULATION (EU) 2017/745 on medical devices)
- Placed on the market
- Turkey
- Market available
- Austria:2015-12-31~None, Belgium:2015-12-31~None, Bulgaria:2015-12-31~None, Croatia:2015-12-31~None, Cyprus:2015-12-31~None, Czechia:2015-12-31~None, Denmark:2015-12-31~None, Estonia:2015-12-31~None, Finland:2015-12-31~None, France:2015-12-31~None, Germany:2015-12-31~None, Greece:2015-12-31~None, Hungary:2015-12-31~None, Iceland:2015-12-31~None, Ireland:2015-12-31~None, Italy:2015-12-31~None, Latvia:2015-12-31~None, Liechtenstein:2015-12-31~None, Lithuania:2015-12-31~None, Luxembourg:2015-12-31~None, Malta:2015-12-31~None, Netherlands:2015-12-31~None, Norway:2015-12-31~None, Poland:2015-12-31~None, Portugal:2015-12-31~None, Romania:2015-12-31~None, Slovakia:2015-12-31~None, Slovenia:2015-12-31~None, Spain:2015-12-31~None, Sweden:2015-12-31~None, Turkey:2015-12-31~None, United Kingdom (Northern Ireland only):2015-12-31~None
- Human tissues
- No
- Animal tissues
- No
TRAYS, BASKETS, TUBS FOR STERILISATION AND THEIR COMPONENTS
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 08681092602321 and manufactured by FATMA CEYLAN- CEYLAN MEDİKAL İMALAT İTHALAT İHRACAT DIŞ TİCARET in Turkey.
This page provides complete registration details including trade name (CEYLAN), 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.