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Access Cann Glenoid Reamer LG - ARCSA Registration d53053773c10573c49f513a3818ca0bb

Access comprehensive regulatory information for Access Cann Glenoid Reamer LG in the Ecuador medical device market through Pure Global AI's free database. This II medical device is registered under ARCSA ID d53053773c10573c49f513a3818ca0bb and manufactured by BIOMET ORTHOPEDICS. The device was registered on September 07, 2017.

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
II
d53053773c10573c49f513a3818ca0bb
Access Cann Glenoid Reamer LG
ARCSA ID: d53053773c10573c49f513a3818ca0bb
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Device Classification
Risk Class
II
Product Type
Invasive
Brand Name
Biomet Orthopedics
Commercial Name
Instruments for Implantation of Theses, Orthopedics
Sterilization Method
STEAM AUTOCLAVE STERILIZATION
Registration Information
Analysis ID
d53053773c10573c49f513a3818ca0bb
Registration Date
September 07, 2017
Expiration Date
September 07, 2027
Creation Date
November 23, 2022
Product Use

THIS INSTRUMENTATION IS INDICATED TO FACILITATE THE PROPER IMPLANTATION OF THE PROSTHETIC OR FIXING COMPONENTS.

Manufacturer
City
WARSAW
Country
UNITED STATES
Address
56 EAST BELL DRIVE PO BOX 587
Product Owner
Name
BIOMET ORTHOPEDICS
Country
UNITED STATES
Authorized Representative
Address
CATALINA ALDAZ N34 131 AND PORTUGAL BUILDING LA SUIZA FLOOR 3
Phone
23331183