Peg Guide Non-Windowed - ARCSA Registration 065910d43d9bd96c5a748cb3ca022573
Access comprehensive regulatory information for Peg Guide Non-Windowed in the Ecuador medical device market through Pure Global AI's free database. This I medical device is registered under ARCSA ID 065910d43d9bd96c5a748cb3ca022573 and manufactured by TRIMED INC. The device was registered on September 03, 2018.
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
065910d43d9bd96c5a748cb3ca022573
Peg Guide Non-Windowed
ARCSA ID: 065910d43d9bd96c5a748cb3ca022573
Device Classification
Risk Class
I
Product Type
Invasive
Brand Name
TRIMED
Commercial Name
INSTRUMENTS FOR IMPLANTATION OF PROSTHESES
Sterilization Method
NON-STERILE STERILIZED PRIOR TO USE WITH STEAM
Registration Information
Analysis ID
065910d43d9bd96c5a748cb3ca022573
Registration Date
September 03, 2018
Expiration Date
September 03, 2023
Creation Date
June 30, 2022
Product Use
IMPLANTATION OF PLATES, ORTHOPEDIC SCREWS
Manufacturer
Name
TRIMED INCCity
SANTA CLARITA
Country
UNITED STATES
Address
27533 AVENUE HOPKINS SANTA CLARITA, CA USA 91355
Product Owner
Name
TRIMED INC
Country
UNITED STATES
Authorized Representative
Address
AV. 12 DE OCTUBRE N24-739 Y AV COLON TORRE BOREAL PISO 1 OF 103
Phone
23945303