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SUPRATHEL® - ARCSA Registration f1a69f57963ae926bce9824253601e31

Access comprehensive regulatory information for SUPRATHEL® in the Ecuador medical device market through Pure Global AI's free database. This IV medical device is registered under ARCSA ID f1a69f57963ae926bce9824253601e31 and manufactured by POLYMEDICS INNOVATIONS GMBH. The device was registered on February 14, 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
f1a69f57963ae926bce9824253601e31
SUPRATHEL®
ARCSA ID: f1a69f57963ae926bce9824253601e31
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Device Classification
Risk Class
IV
Product Type
Invasive
Brand Name
SUPRATHEL®
Commercial Name
Grafts, Skin, Artificial
Registration Information
Analysis ID
f1a69f57963ae926bce9824253601e31
Registration Date
February 14, 2017
Expiration Date
February 14, 2027
Product Use

IT IS USED IN EPIDERMAL AND DERMAL WOUNDS, SUCH AS ABRASIONS, SKIN DONOR AREAS FOR GRAFTING, SECOND-DEGREE BURNS WITH THE PRESENCE OF THIRD-DEGREE AREAS.

Manufacturer
Country
GERMANY
Address
HEERWEG 15 D, 73770 DENKENDORF
Product Owner
Name
POLYMEDICS INNOVATIONS GMBH
Country
GERMANY
Authorized Representative
Address
AV. REPUBLICA DEL SALVADOR N34-461 AND AV. PORTUGAL
Phone
22247143