EUDAMED registration G1551435110NoProbe Double Ended 17cm
- Risk class
- Class I
- CND nomenclatures code
- L159003
- Trade name
- Probe Double Ended 17cm
- Implantable
- No
- Reusable
- Yes
- Measuring function
- No
- Primary DI
- G1551435110
- Basic UDI
- ++G1551435115D
- Version date
- September 03, 2024
- Manufacturer last update
- August 01, 2022
- Active status
- No
- Manufacturer name
- Nadir & CO
- Country
- Pakistan
- Country type
- NON_EU
- Address
- Ugoki Road, Opp: Small Industrial Estate Shahab Pura 51310 Sialkot
- info@nadirco.com
- SRN
- DE-AR-000008078
- Country
- Germany
- Address
- 6 Hans Bunte Strasse Heidelberg
- info@antex-medi-solution.de
- Telephone
- +4915678612574
- Competent authority
- DE/CA38 - Regierungspräsidium Karlsruhe
- Applicable legislation
- MDR (REGULATION (EU) 2017/745 on medical devices)
- Placed on the market
- Austria
- Market available
- 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, Austria:None~None, Belgium:None~None, Bulgaria:None~None, Croatia:None~None, Cyprus:None~None, Czechia:None~None
- Human tissues
- No
- Animal tissues
- No
DENTAL AND PERIODONTAL PROBES AND EXPLORERS, REUSABLE
Access comprehensive regulatory information for Probe Double Ended 17cm 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 G1551435110 and manufactured by Nadir & CO in Pakistan.
This page provides complete registration details including trade name (Probe Double Ended 17cm), manufacturer information, authorized representative details, competent authority (DE/CA38 - Regierungspräsidium Karlsruhe), 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.