DURAL REPAIR PATCH (Trade Name: NeoDura™) - ARCSA Registration 17f66a6c8aa43ebe0d9c941611cd50ce
Access comprehensive regulatory information for DURAL REPAIR PATCH (Trade Name: NeoDura™) in the Ecuador medical device market through Pure Global AI's free database. This IV medical device is registered under ARCSA ID 17f66a6c8aa43ebe0d9c941611cd50ce and manufactured by MEDPRIN BIOTECH GMBH. The device was registered on August 02, 2022.
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
17f66a6c8aa43ebe0d9c941611cd50ce
DURAL REPAIR PATCH
(Trade Name: NeoDura™)
ARCSA ID: 17f66a6c8aa43ebe0d9c941611cd50ce
Device Classification
Risk Class
IV
Product Type
Invasive
Brand Name
NeoDura™ / ReDura™
Commercial Name
DURA MATER IMPLANTS
Sterilization Method
GAMMA RADIATION
Registration Information
Analysis ID
17f66a6c8aa43ebe0d9c941611cd50ce
Registration Date
August 02, 2022
Expiration Date
August 02, 2027
Creation Date
February 08, 2022
Product Use
IT IS INDICATED AS A DURAL REPAIR PATCH FOR THE SURGICAL REPAIR OF DURAL DEFECTS.
Manufacturer
Product Owner
Name
MEDPRIN BIOTECH GMBH
Country
GERMANY
Authorized Representative
Address
MANUELA SAENZ N34-259 AND ABELARDO MONCAYO
Phone
2442768