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Regenerative Dural Repair Patch (Trade name: ReDura) - ARCSA Registration 907b61b6bd9aa5474b269ef039677934

Access comprehensive regulatory information for Regenerative Dural Repair Patch (Trade name: ReDura) in the Ecuador medical device market through Pure Global AI's free database. This IV medical device is registered under ARCSA ID 907b61b6bd9aa5474b269ef039677934 and manufactured by MEDPRIN BIOTECH GMBH. The device was registered on July 20, 2017.

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
907b61b6bd9aa5474b269ef039677934
Regenerative Dural Repair Patch (Trade name: ReDura)
ARCSA ID: 907b61b6bd9aa5474b269ef039677934
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Device Classification
Risk Class
IV
Product Type
Invasive
Brand Name
ReDura / NeoDura
Commercial Name
Dura Mater Implants
Registration Information
Analysis ID
907b61b6bd9aa5474b269ef039677934
Registration Date
July 20, 2017
Expiration Date
July 20, 2027
Product Use

REGENERATIVE DURA MATER REPAIR PATCH FOR SURGICAL REPAIR OPERATIONS FOR DESTRUCTIVE DURA MATER DEFECTS.

Manufacturer
Country
GERMANY
Address
GUTLEUTSTRASSE 163-167, 60327
Product Owner
Name
MEDPRIN BIOTECH GMBH
Country
GERMANY
Authorized Representative
Address
KENNEDY NORTH MIGUEL H. ALCIVAR SOLAR 11
Phone
45104823