DURAL REPAIR PATCH NEODURA - ARCSA Registration 968b0b2200a5ea42b7a1d74b9f9f6e84
Access comprehensive regulatory information for DURAL REPAIR PATCH NEODURA in the Ecuador medical device market through Pure Global AI's free database. This IV medical device is registered under ARCSA ID 968b0b2200a5ea42b7a1d74b9f9f6e84 and manufactured by MEDPRIN BIOTECH GMBH. The device was registered on April 28, 2021.
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
IV
968b0b2200a5ea42b7a1d74b9f9f6e84
DURAL REPAIR PATCH NEODURA
ARCSA ID: 968b0b2200a5ea42b7a1d74b9f9f6e84
Device Classification
Risk Class
IV
Product Type
Invasive
Brand Name
MEDPRIN BIOTECH
Commercial Name
Dura Mater Implants
Sterilization Method
GAMMA RADIATION
Registration Information
Analysis ID
968b0b2200a5ea42b7a1d74b9f9f6e84
Registration Date
April 28, 2021
Expiration Date
April 28, 2026
Creation Date
April 28, 2021
Product Use
IT IS INDICATED AS A DURAL REPAIR PATCH FOR THE SURGICAL REPAIR OF DURAL DEFECTS.
Manufacturer
City
FRANKFURT
Country
GERMANY
Address
GUTLEUTSTRABE 163-167, 60327 FRANKFURT AM MAIN
Product Owner
Name
MEDPRIN BIOTECH GMBH
Country
GERMANY
Authorized Representative