ACLERA ALISADORA - ARCSA Registration 56e99600796e35ae6ea62ffff55dc702
Access comprehensive regulatory information for ACLERA ALISADORA in the Ecuador medical device market through Pure Global AI's free database. This I medical device is registered under ARCSA ID 56e99600796e35ae6ea62ffff55dc702 and manufactured by SURGIVAL & CO. S.A.U.. The device was registered on November 08, 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
56e99600796e35ae6ea62ffff55dc702
ACLERA ALISADORA
ARCSA ID: 56e99600796e35ae6ea62ffff55dc702
Local name: FRESA ALISADORA
Device Classification
Risk Class
I
Product Type
Invasive
Brand Name
QUARTER, KAREY, SURGIVAL
Commercial Name
Instruments for Prosthesis Implantation
Sterilization Method
NON-STERILE
Registration Information
Analysis ID
56e99600796e35ae6ea62ffff55dc702
Registration Date
November 08, 2022
Expiration Date
November 08, 2027
Creation Date
August 11, 2022
Product Use
INSTRUMENTS FOR THE IMPLANTATION OF THE KAREY FEMORAL COMPONENT WITHIN A TOTAL OR PARTIAL HIP REPLACEMENT
Manufacturer
City
VALENCE
Country
SPAIN
Address
C/ LEONARDO DA VINCI, 12-14, PARQUE TECNOLOGICO 46980 PATERNA-VALENCIA, SPAIN
Product Owner
Name
SURGIVAL & CO. S.A.U.
Country
SPAIN
Authorized Representative