HA-SET063: Sterile, Single Use, Set Cataracte 4 instruments
- Risk class
- Class IIa
- CND nomenclatures code
- Q021113
- Trade name
- HASA OPTIX
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- 05404027449326
- Basic UDI
- B-05404027449326
- Version date
- March 07, 2025
- Manufacturer last update
- January 16, 2023
- Active status
- No
- Manufacturer name
- HASA OPTIX
- Country
- Belgium
- Country type
- EU_MEMBER_STATE
- Address
- 523 Avenue Louise Brussels
- info@hasaoptix.com
- Competent authority
- Federaal Agentschap voor Geneesmiddelen en Gezondheidsproducten/ Afdeling Gezondheidsproducten
- Applicable legislation
- MDD (Directive 93/42/EEC on Medical Devices)
- Placed on the market
- Belgium
- Market available
- Austria:None~None, Belgium:None~None, Bulgaria:None~None, Croatia:None~None, Cyprus:None~None, Czechia:None~None, Denmark:None~None, Estonia:None~None, Finland:None~None, France:None~None, Germany:None~None, Greece:None~None, Hungary:None~None, Iceland:None~None, Ireland:None~None, Italy:None~None, Latvia:None~None, Liechtenstein:None~None, Lithuania:None~None, Luxembourg:None~None, Malta:None~None, Netherlands:None~None, Norway:None~None, Poland:None~None, Portugal:None~None, Romania:None~None, Slovakia:None~None, Slovenia:None~None, Spain:None~None, Sweden:None~None, Türkiye:None~None, United Kingdom (Northern Ireland only):None~None
- Human tissues
- No
- Animal tissues
- No
OPHTHALMIC SURGERY INSTRUMENT KITS, SINGLE-USE
Access comprehensive regulatory information for HA-SET063: Sterile, Single Use, Set Cataracte 4 instruments in the European Union medical device market through Pure Global AI's free database. This Class IIa device is registered with EU EUDAMED under Primary DI 05404027449326 and manufactured by HASA OPTIX in Belgium.
This page provides complete registration details including trade name (HASA OPTIX), manufacturer information, competent authority (Federaal Agentschap voor Geneesmiddelen en Gezondheidsproducten/ Afdeling Gezondheidsproducten), 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.