STERILIZATION CONTAINER SYSTEMS
- Risk class
- Class I
- CND nomenclatures code
- S010401
- Trade name
- ATLAS
- Implantable
- No
- Reusable
- Yes
- Measuring function
- No
- Primary DI
- 08683779048675
- Basic UDI
- 8683255ATLAS55KNTYNRNE
- Version date
- February 27, 2024
- Manufacturer last update
- February 05, 2024
- Active status
- No
- Manufacturer name
- ATLAS CERRAHİ ALETLER LTD. ŞTİ.
- Country
- Turkey
- Country type
- EU_EXTENDED
- Address
- 1004 CAD. 55300 SAMSUN
- bilgi@atlascerrahialetler.com
- 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 08683779048675 and manufactured by ATLAS CERRAHİ ALETLER LTD. ŞTİ. in Turkey.
This page provides complete registration details including trade name (ATLAS), 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.