Dental Abutment
- Risk class
- Class IIb
- CND nomenclatures code
- P01020180
- Trade name
- WD Free-rotation Titanium/Plastic Abutment
- Implantable
- Yes
- Reusable
- No
- Measuring function
- No
- Primary DI
- D-DEMF000009412MWD3097C7
- Basic UDI
- B-DEMF000009412MWD3097C7
- Version date
- June 21, 2022
- Manufacturer last update
- November 17, 2021
- Active status
- No
- Manufacturer name
- MEDIGMA BIOMEDICAL GMBH
- Country
- Germany
- Country type
- EU_MEMBER_STATE
- Address
- 10 Siemensstraße Wehingen
- office@medigma-implants.com
- Competent authority
- DE/CA39, Regierungspräsidium Freiburg Referat 25
- Applicable legislation
- MDD (Directive 93/42/EEC on Medical Devices)
- Placed on the market
- Turkey
- 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, Spain:None~None, Finland:None~None, France:None~None, Greece: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, Poland:None~None, Portugal:None~None, Romania:None~None, Sweden:None~None, Slovenia:None~None, Slovakia:None~None, United Kingdom (Northern Ireland only):None~None, Turkey:2017-06-27~None
- Human tissues
- No
- Animal tissues
- No
DENTAL IMPLANTS - ACCESSORIES
Access comprehensive regulatory information for Dental Abutment 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 D-DEMF000009412MWD3097C7 and manufactured by MEDIGMA BIOMEDICAL GMBH in Germany.
This page provides complete registration details including trade name (WD Free-rotation Titanium/Plastic Abutment), manufacturer information, competent authority (DE/CA39, Regierungspräsidium Freiburg Referat 25), 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.