Restorative dental hand instrument
- Risk class
- Class I
- CND nomenclatures code
- Q01010199
- Trade name
- LM Build-up Trimmer
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- 06438311707471
- Basic UDI
- 6438311RESTO102Y
- Version date
- March 06, 2025
- Manufacturer last update
- November 03, 2021
- Active status
- No
- Manufacturer name
- LM-Instruments Oy
- Country
- Finland
- Country type
- EU_MEMBER_STATE
- Address
- 8 Norrbyn rantatie Parainen
- info@lm-dental.com
- Competent authority
- Finnish Medicines Agency, Supervision and licences, Medical Device Unit
- Applicable legislation
- MDR (REGULATION (EU) 2017/745 on medical devices)
- Placed on the market
- Finland
- Market available
- Finland:None~None, 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, 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, Türkiye:None~None, United Kingdom (Northern Ireland only):None~None
- Human tissues
- No
- Animal tissues
- No
DENTAL RESTORATION DEVICES - OTHER
Access comprehensive regulatory information for Restorative dental hand instrument 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 06438311707471 and manufactured by LM-Instruments Oy in Finland.
This page provides complete registration details including trade name (LM Build-up Trimmer), manufacturer information, competent authority (Finnish Medicines Agency, Supervision and licences, Medical Device Unit), 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.