577nm LIO
- Risk class
- Class IIb
- CND nomenclatures code
- Z12120199
- Trade name
- 577nm LIO
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- 05055272720380
- Basic UDI
- B-05055272720380
- Version date
- March 04, 2025
- Manufacturer last update
- September 10, 2024
- Active status
- Yes
- Manufacturer name
- Keeler Ltd
- Country
- United Kingdom (ex Northern Ireland)
- Country type
- NON_EU
- Address
- Clewer Hill Road Windsor
- regulatory@keeler.co.uk
- SRN
- ES-AR-000001559
- Country
- Spain
- Address
- 453 Colom, Terrassa
- info@visiometrics.com
- Competent authority
- Agencia Española de Medicamentos y Productos Sanitarios
- Applicable legislation
- MDD (Directive 93/42/EEC on Medical Devices)
- Placed on the market
- Netherlands
- Market available
- Netherlands:None~None
- Human tissues
- No
- Animal tissues
- No
OPHTALMOLOGY ASSESSMENTS AND DIAGNOSIS INSTRUMENTS – OTHER
Access comprehensive regulatory information for 577nm LIO 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 05055272720380 and manufactured by Keeler Ltd in United Kingdom (ex Northern Ireland).
This page provides complete registration details including trade name (577nm LIO), manufacturer information, authorized representative details, competent authority (Agencia Española de Medicamentos y Productos Sanitarios), 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.