CONSERVATIVE
- Risk class
- Class I
- CND nomenclatures code
- L07080102
- Trade name
- ASELTECH
- Implantable
- No
- Reusable
- Yes
- Measuring function
- No
- Primary DI
- 08681376027406
- Basic UDI
- 8681376ASELTECH201524AM
- Version date
- January 18, 2024
- Manufacturer last update
- February 06, 2024
- Active status
- No
- Manufacturer name
- Asel Tibbi Aletler A.S.
- Country
- Turkey
- Country type
- EU_EXTENDED
- Address
- 255/1 Koprubasi Mah. Selanik Cad. Tekkekoy 55300 Samsun
- info@aseltech.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
- 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, 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
- Human tissues
- No
- Animal tissues
- No
GENERIC VASCULAR CLAMPING ANGIOSTATS AND FORCEPS, REUSABLE
Access comprehensive regulatory information for CONSERVATIVE 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 08681376027406 and manufactured by Asel Tibbi Aletler A.S. in Turkey.
This page provides complete registration details including trade name (ASELTECH), 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.