ST.LEGER NEO MOBILE BEARING P/S TIBIAL INSERT (XL) 65mm 13mm
- Risk class
- Class III
- CND nomenclatures code
- P090903020201
- Trade name
- COVISION
- Implantable
- Yes
- Reusable
- No
- Measuring function
- No
- Primary DI
- 05051659062692
- Basic UDI
- B-05051659062692
- Version date
- June 17, 2023
- Manufacturer last update
- November 24, 2022
- Active status
- No
- Manufacturer name
- Covision Medical Technologies Ltd.
- Country
- United Kingdom (ex Northern Ireland)
- Country type
- NON_EU
- Address
- Lawn Rd., Carlton Industrial Park, Carlton In Lindrick, Worksop Nottinghamshire
- mike.rimmer@covision-medical.co.uk
- SRN
- IE-AR-000031129
- Country
- Ireland
- Address
- Coliemore House Coliemore Road Dublin
- cmtireland@covision-medical.co.uk
- Telephone
- +44(0)1909733737
- Competent authority
- Turkish Medicine and Medical Devices Agency
- Applicable legislation
- MDD (Directive 93/42/EEC on Medical Devices)
- Placed on the market
- Austria
- 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
BICOMPARTMENTAL PRIMARY IMPLANT MOBILE BEARING TIBIAL INSERTS
Access comprehensive regulatory information for ST.LEGER NEO MOBILE BEARING P/S TIBIAL INSERT (XL) 65mm 13mm in the European Union medical device market through Pure Global AI's free database. This Class III device is registered with EU EUDAMED under Primary DI 05051659062692 and manufactured by Covision Medical Technologies Ltd. in United Kingdom (ex Northern Ireland).
This page provides complete registration details including trade name (COVISION), manufacturer information, authorized representative details, 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.