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REGENERATIVE DURAL REPAIR PATCH (Trade Name: ReDura™) - ARCSA Registration fa5245f125b816ecd7bc2c944504dc74

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 fa5245f125b816ecd7bc2c944504dc74 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
fa5245f125b816ecd7bc2c944504dc74
REGENERATIVE DURAL REPAIR PATCH (Trade Name: ReDura™)
ARCSA ID: fa5245f125b816ecd7bc2c944504dc74
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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
fa5245f125b816ecd7bc2c944504dc74
Registration Date
August 02, 2022
Expiration Date
August 02, 2027
Creation Date
February 08, 2022
Product Use

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

Manufacturer
City
FRANKFURT AM MAIN
Country
GERMANY
Address
GUTLEUSTRABE 163-167
Product Owner
Name
MEDPRIN BIOTECH GMBH
Country
GERMANY
Authorized Representative
Address
MANUELA SAENZ N34-259 AND ABELARDO MONCAYO
Phone
2442768