GRYPHON PEEK ANCHOR - ARCSA Registration 42dff074186af73a3fb304e651de5058
Access comprehensive regulatory information for GRYPHON PEEK ANCHOR in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID 42dff074186af73a3fb304e651de5058 and manufactured by MEDOS SARL. The device was registered on February 01, 2019.
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.
Free Database
Powered by Pure Global AI
ARCSA Official Data
III
42dff074186af73a3fb304e651de5058
GRYPHON PEEK ANCHOR
ARCSA ID: 42dff074186af73a3fb304e651de5058
Device Classification
Risk Class
III
Product Type
Invasive
Brand Name
GRYPHON™
Commercial Name
SUTURE ANCHORS
Sterilization Method
ETHYLENE OXIDE
Registration Information
Analysis ID
42dff074186af73a3fb304e651de5058
Registration Date
February 01, 2019
Expiration Date
February 01, 2024
Creation Date
January 02, 2019
Product Use
THE GRYPHON PEEK ANCHOR IS DESIGNED FOR SHOULDER REPAIR, FOOT/ANKLE REPAIR, KNEE AND HIP REPAIR AND ELBOW RECONSTRUCTION.
Manufacturer
Product Owner
Name
MEDOS INTERNATIONAL SARL
Country
SWITZERLAND
Authorized Representative
Address
AV. RODRIGUEZ CHAVEZ, COLON BUSINESS PARK, CORPORATE BUILDING 2
Phone
6001303