03700712434496
Volista
Maquet SAS·Class I·EU EUDAMED·Trade name: VCSII66SF SB0810Yes
Device classification
- Risk class
- Class I
- CND nomenclatures code
- Z12010701
- Trade name
- VCSII66SF SB0810
- Implantable
- No
- Reusable
- No
- Measuring function
- No
Registration information
- Primary DI
- 03700712434496
- Basic UDI
- 3700712432607S4
- Version date
- December 10, 2024
- Manufacturer last update
- February 04, 2022
- Active status
- Yes
Manufacturer
- Manufacturer name
- Maquet SAS
- Country
- France
- Country type
- EU_MEMBER_STATE
- Address
- Parc de Limère - Avenue de la Pomme de Pin ARDON
- pascal.jay@getinge.com
Regulatory information
- Competent authority
- Agence Nationale de Sécurité du Médicament et des Produits de Santé
- Applicable legislation
- MDR (REGULATION (EU) 2017/745 on medical devices)
- Placed on the market
- France
- 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, 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
Device characteristics
- Human tissues
- No
- Animal tissues
- No
Device description (EMDN)
FIXED SCIALYTIC LAMPS
About this record
Access comprehensive regulatory information for Volista 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 03700712434496 and manufactured by Maquet SAS in France.
This page provides complete registration details including trade name (VCSII66SF SB0810), manufacturer information, competent authority (Agence Nationale de Sécurité du Médicament et des Produits de Santé), 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.