4d4f6ce90537d93937e329c591843c2d
GRAEFE Cataract
ALBERT HEISS GMBH & CO. KG·I·Ecuador ARCSA·Registered December 07, 2022
Device classification
- Risk class
- I
- Product type
- Invasive
- Brand name
- ALBERT HEISS
- Commercial name
- Instruments for Microsurgery
- Sterilization method
- NON-STERILE
Registration information
- Analysis ID
- 4d4f6ce90537d93937e329c591843c2d
- Registration date
- December 07, 2022
- Expiration date
- December 07, 2027
- Creation date
- July 12, 2022
Manufacturer
- City
- TUTTLINGEN
- Country
- GERMANY
- Address
- STOCKACHER STRASSE 138 78532 TUTTLINGEN ALEMANIA
Product owner
- Name
- ALBERT HEISS GMBH & CO. KG
- Country
- GERMANY
Authorized representative
- Address
- SAN ISIDRO DEL INCA / B SN Y C
- Phone
- 2380161
Product use
MEDICAL INSTRUMENTS FOR OPHTHALMIC SURGERY
About this record
Access comprehensive regulatory information for GRAEFE Cataract in the Ecuador medical device market through Pure Global AI's free database. This I medical device is registered under ARCSA ID 4d4f6ce90537d93937e329c591843c2d and manufactured by ALBERT HEISS GMBH & CO. KG. The device was registered on December 07, 2022.
This page provides complete registration details including product type (Invasive), manufacturer information, authorized representative details, and regulatory compliance data from the official Ecuador ARCSA medical device database. Pure Global AI offers free access to Ecuador's complete medical device registry.