GRAEFE Cataract - ARCSA Registration 4d4f6ce90537d93937e329c591843c2d
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.
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ARCSA Official Data
I
4d4f6ce90537d93937e329c591843c2d
GRAEFE Cataract
ARCSA ID: 4d4f6ce90537d93937e329c591843c2d
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
Product Use
MEDICAL INSTRUMENTS FOR OPHTHALMIC SURGERY
Manufacturer
City
TUTTLINGEN
Country
GERMANY
Address
STOCKACHER STRASSE 138 78532 TUTTLINGEN ALEMANIA
Product Owner
Name
ALBERT HEISS GMBH & CO. KG
Country
GERMANY
Authorized Representative