GRYPHON™ with PROKNOT™ TECHNOLOGY - ARCSA Registration 946dd57a16b4361430c1e293158185ca
Access comprehensive regulatory information for GRYPHON™ with PROKNOT™ TECHNOLOGY in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID 946dd57a16b4361430c1e293158185ca and manufactured by MEDOS SARL. The device was registered on February 01, 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.
Free Database
Powered by Pure Global AI
ARCSA Official Data
III
946dd57a16b4361430c1e293158185ca
GRYPHON™ with PROKNOT™ TECHNOLOGY
ARCSA ID: 946dd57a16b4361430c1e293158185ca
Device Classification
Risk Class
III
Product Type
Invasive
Brand Name
GRYPHON™
Commercial Name
Suture Anchors
Sterilization Method
ETHYLENE OXIDE
Registration Information
Analysis ID
946dd57a16b4361430c1e293158185ca
Registration Date
February 01, 2018
Expiration Date
February 01, 2023
Creation Date
January 02, 2018
Product Use
THE GRYPHON ANCHOR WITH PROKNOT IS DESIGNED FOR SHOULDER AND HIP REPAIR.
Manufacturer
Product Owner
Name
DEPUY MITEK INC.
Country
UNITED STATES
Authorized Representative
Address
AV. RODRIGO CHAVEZ GONZALEZ PARQUE EMPRESARIAL COLON EDIFICIO CORPORATIVO 2 PISO 6
Phone
26001303