SCALPEL HANDLE 135mm
- Risk class
- Class I
- CND nomenclatures code
- L1204
- Trade name
- IDOL
- Implantable
- No
- Reusable
- Yes
- Measuring function
- No
- Primary DI
- 08699241083723
- Basic UDI
- 86992410TD01-02J3
- Version date
- June 19, 2023
- Manufacturer last update
- July 25, 2022
- Active status
- No
- Manufacturer name
- İDOL HASTANE ÜRÜN. SAN. VE TİC. A.Ş.
- Country
- Turkey
- Country type
- EU_EXTENDED
- Address
- 39/1 Sk. Altınova Sinan Mh. antalya
- info@idolcerrahi.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: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, Turkey:None~None, United Kingdom (Northern Ireland only):None~None
- Human tissues
- No
- Animal tissues
- No
LAPAROSCOPIC AND THORACOSCOPIC SURGERY FORCEPS REUSABLE
Access comprehensive regulatory information for SCALPEL HANDLE 135mm 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 08699241083723 and manufactured by İDOL HASTANE ÜRÜN. SAN. VE TİC. A.Ş. in Turkey.
This page provides complete registration details including trade name (IDOL), 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.