CONTAINER 3D+, OPTIONAL TUBES - ARCSA Registration 3d2fc12106f6ac9fcf5c58fa1e183a4e
Access comprehensive regulatory information for CONTAINER 3D+, OPTIONAL TUBES in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID 3d2fc12106f6ac9fcf5c58fa1e183a4e and manufactured by Spineway S.A.S.. The device was registered on August 16, 2012.
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
III
3d2fc12106f6ac9fcf5c58fa1e183a4e
CONTAINER 3D+, OPTIONAL TUBES
ARCSA ID: 3d2fc12106f6ac9fcf5c58fa1e183a4e
Device Classification
Risk Class
III
Product Type
Invasive
Brand Name
Spineway
Commercial Name
BODY PROSTHESIS AND MATERIAL FOR OSTEOSYNTHESIS TO BE USED IN ORTHOPEDICS, TRAUMATOLOGY, NEUROSURGERY (PLATES, SCREWS, NAILS, ETC.)
Sterilization Method
GAMMA RADIATION
Registration Information
Analysis ID
3d2fc12106f6ac9fcf5c58fa1e183a4e
Registration Date
August 16, 2012
Expiration Date
August 16, 2027
Creation Date
February 06, 2022
Product Use
FOR SPINAL FUSION INTERVENTIONS
Manufacturer
Product Owner
Name
Spineway S.A.S.
Country
FRANCE
Authorized Representative
Address
PASSAGE LOS ANGELES E 414 AND GERMANY EDFICIO DA VINCE OFFICE 108
Phone
2235634