Metal and plastic spectacle frames without lenses
- Risk class
- Class I
- CND nomenclatures code
- Q02100202
- Trade name
- EYEVAN
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- 04582669024284
- Basic UDI
- 458266902RXCMBMW
- Version date
- November 22, 2024
- Manufacturer last update
- September 13, 2022
- Active status
- No
- Manufacturer name
- EYEVAN Inc.
- Country
- Japan
- Country type
- NON_EU
- Address
- 1-15-33 Minami-Aoyama Minato-Ku
- m.yamagishi@eyevan.co.jp
- Name
- EYEVAN Europe
- SRN
- FR-AR-000025678
- Country
- France
- Address
- 41 Rue Boissy d'Anglas Pairs
- m.yamagishi@eyevan.co.jp
- Telephone
- +33 1 84 25 05 15
- 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
- Human tissues
- No
- Animal tissues
- No
PLASTIC SPECTACLE FRAMES WITHOUT LENSES
Access comprehensive regulatory information for Metal and plastic spectacle frames without lenses 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 04582669024284 and manufactured by EYEVAN Inc. in Japan.
This page provides complete registration details including trade name (EYEVAN), manufacturer information, authorized representative details, 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.