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Membracel - Membrana Regeneradora Porosa -Poro Medio - ARCSA Registration 74442ac3052f856cc215505e38a8d593

Access comprehensive regulatory information for Membracel - Membrana Regeneradora Porosa -Poro Medio in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID 74442ac3052f856cc215505e38a8d593 and manufactured by FLIGHT PHARMA LTDA - ME. The device was registered on March 29, 2023.

This page provides complete registration details including product type (No 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
74442ac3052f856cc215505e38a8d593
Membracel - Membrana Regeneradora Porosa -Poro Medio
ARCSA ID: 74442ac3052f856cc215505e38a8d593
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Device Classification
Risk Class
III
Product Type
No Invasive
Brand Name
Membracel
Commercial Name
MATERIALS TO RECONSTRUCT TISSUES
Registration Information
Analysis ID
74442ac3052f856cc215505e38a8d593
Registration Date
March 29, 2023
Expiration Date
March 29, 2028
Product Use

POROUS REGENERATIVE MEMBRANE IS A CRYSTALLINE CELLULOSE MEMBRANE SYNTHESIZED BY THE BACTERIUM ACETOBACTER XYLINUM, WITH POROSITY ARTIFICIALLY DEVELOPED TO ALLOW DRAINAGE OF EXUDATE. THE MEMBRANE ACTS AS A TEMPORARY SUBSTITUTE FOR THE SKIN AND IS INDICATED FOR THE TREATMENT OF LESIONS RESULTING FROM THE LOSS OF THE EPITHELIUM THAT ARE CHARACTERIZED AS SUPERFICIAL OR DEEP WOUNDS OF THE SKIN, WITH LITTLE OR ABUNDANT EXUDATION

Manufacturer
City
CURITIBA
Country
BRAZIL
Address
RUA CARLOS MULLER, B. 315-INDUSTRIAL CITY, CURITIBA - PR
Product Owner
Name
FLIGHT PHARMA LTDA - ME
Country
BRAZIL
Authorized Representative
Address
AV. REPUBLICA DEL SALVADOR N34-461 AND AV. PORTUGAL
Phone
22247143