REVERSER
- Risk class
- Class I
- CND nomenclatures code
- L149012
- Trade name
- S.C.A
- Implantable
- No
- Reusable
- Yes
- Measuring function
- No
- Primary DI
- 08698980482217
- Basic UDI
- 868086255S.C.A3545TQ
- Version date
- May 03, 2024
- Manufacturer last update
- January 06, 2022
- Active status
- No
- Manufacturer name
- SAMSUN CERRAHİ ALETLER SANAYİ VE TİCARET LİMİTED ŞİRKETİ
- Country
- Türkiye
- Country type
- EU_EXTENDED
- Address
- 47 / 49 Kirazlık Mahallesi Sahil Caddesi Tekkeköy SAMSUN
- info@sca.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: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, Türkiye:2015-12-31~None, United Kingdom (Northern Ireland only):2015-12-31~None
- Human tissues
- No
- Animal tissues
- No
ENT SURGERY PUNCHES, REUSABLE
Access comprehensive regulatory information for REVERSER 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 08698980482217 and manufactured by SAMSUN CERRAHİ ALETLER SANAYİ VE TİCARET LİMİTED ŞİRKETİ in Türkiye.
This page provides complete registration details including trade name (S.C.A), 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.