ANT REF CUT GD SZ 12 CASEBRKT - ARCSA Registration a94c2d002c2d6a762a4d704deba725ab
Access comprehensive regulatory information for ANT REF CUT GD SZ 12 CASEBRKT in the Ecuador medical device market through Pure Global AI's free database. This I medical device is registered under ARCSA ID a94c2d002c2d6a762a4d704deba725ab and manufactured by ZIMMER, INC. The device was registered on October 05, 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
a94c2d002c2d6a762a4d704deba725ab
ANT REF CUT GD SZ 12 CASEBRKT
ARCSA ID: a94c2d002c2d6a762a4d704deba725ab
Device Classification
Risk Class
I
Product Type
Invasive
Brand Name
Room
Commercial Name
Instruments for Prosthesis Implantation, Orthopedic
Sterilization Method
NOT STERILE
Registration Information
Analysis ID
a94c2d002c2d6a762a4d704deba725ab
Registration Date
October 05, 2022
Expiration Date
October 05, 2027
Creation Date
May 10, 2022
Product Use
THIS INSTRUMENTATION IS INDICATED TO FACILITATE THE PROPER IMPLANTATION OF THE PROSTHETIC OR FIXING COMPONENTS.
Manufacturer
Product Owner
Name
ZIMMER, INC
Country
UNITED STATES
Authorized Representative
Address
CATALINA ALDAZ N34 131 AND PORTUGAL BUILDING LA SUIZA FLOOR 3
Phone
23331183