Screwdriver
- Risk class
- Class I
- CND nomenclatures code
- L091001
- Implantable
- No
- Reusable
- Yes
- Measuring function
- No
- Primary DI
- 05908447144767
- Basic UDI
- 59084472NL075MS
- Version date
- October 05, 2024
- Manufacturer last update
- March 16, 2021
- Active status
- No
- Manufacturer name
- ChM spółka z ograniczoną odpowiedzialnością
- Country
- Poland
- Country type
- EU_MEMBER_STATE
- Address
- 3B LEWICKIE JUCHNOWIEC KOŚCIELNY
- chm@chm.eu
- Competent authority
- Urząd Rejestracji Produktów Leczniczych
- Applicable legislation
- MDR (REGULATION (EU) 2017/745 on medical devices)
- Placed on the market
- Poland
- Market available
- Austria:None~None, Belgium:None~None, Bulgaria:None~None, Cyprus:None~None, Czechia:None~None, Germany:None~None, Denmark:None~None, Estonia:None~None, Greece:None~None, Spain:None~None, Finland:None~None, France:None~None, Croatia:None~None, Hungary:None~None, Ireland:None~None, Iceland:None~None, Italy:None~None, Liechtenstein:None~None, Lithuania:None~None, Luxembourg:None~None, Latvia:None~None, Malta:None~None, Netherlands:None~None, Norway:None~None, Portugal:None~None, Romania:None~None, Sweden:None~None, Slovenia:None~None, Slovakia:None~None, Türkiye:None~None, United Kingdom (Northern Ireland only):None~None, Poland:None~None
- Human tissues
- No
- Animal tissues
- No
INSTRUMENTS FOR INSERTION AND EXTRACTION OF MATERIALS FOR OSTEOSYNTHESIS, REUSABLE
Access comprehensive regulatory information for Screwdriver 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 05908447144767 and manufactured by ChM spółka z ograniczoną odpowiedzialnością in Poland.
This page provides complete registration details including manufacturer information, competent authority (Urząd Rejestracji Produktów Leczniczych), 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.