TUBULAR FIXATOR ÇUBUK-ÇUBUK KLEMP (TUBULAR FIXATOR ROD-ROD CLAMP) 5 MM
- Risk class
- Class IIb
- CND nomenclatures code
- P09120499
- Trade name
- AYSAM
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- 08698823384906
- Basic UDI
- B-08698823384906
- Version date
- July 02, 2024
- Manufacturer last update
- November 07, 2023
- Active status
- No
- Manufacturer name
- Aysam Ortopedi ve Tıbbi Aletler Sanayi ve Ticaret Limited Şirketi
- Country
- Türkiye
- Country type
- EU_EXTENDED
- Address
- Kirazlik Mh Samsun
- info@aysam.com.tr
- Competent authority
- Turkish Medicine and Medical Devices Agency
- Applicable legislation
- MDD (Directive 93/42/EEC on Medical Devices)
- Placed on the market
- Türkiye
- 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, Türkiye:None~None, United Kingdom (Northern Ireland only):None~None
- Human tissues
- No
- Animal tissues
- No
EXTERNAL BONE FIXATION SYSTEMS - OTHER
Access comprehensive regulatory information for TUBULAR FIXATOR ÇUBUK-ÇUBUK KLEMP (TUBULAR FIXATOR ROD-ROD CLAMP) 5 MM in the European Union medical device market through Pure Global AI's free database. This Class IIb device is registered with EU EUDAMED under Primary DI 08698823384906 and manufactured by Aysam Ortopedi ve Tıbbi Aletler Sanayi ve Ticaret Limited Şirketi in Türkiye.
This page provides complete registration details including trade name (AYSAM), 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.