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Duosynt - ARCSA Registration c9b3614dfb9044adc0c6ba8b6aee2c7a

Access comprehensive regulatory information for Duosynt in the Ecuador medical device market through Pure Global AI's free database. This IV medical device is registered under ARCSA ID c9b3614dfb9044adc0c6ba8b6aee2c7a and manufactured by DENTSCARE LTDA.. The device was registered on August 21, 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
c9b3614dfb9044adc0c6ba8b6aee2c7a
Duosynt
ARCSA ID: c9b3614dfb9044adc0c6ba8b6aee2c7a
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Device Classification
Risk Class
IV
Product Type
Invasive
Brand Name
FGM
Commercial Name
Implantable Membranes for Periodontal Regeneration, Absorbable
Sterilization Method
GAMMA RADIATION
Registration Information
Analysis ID
c9b3614dfb9044adc0c6ba8b6aee2c7a
Registration Date
August 21, 2022
Expiration Date
August 21, 2027
Creation Date
August 21, 2022
Product Use

SYNTHETIC REGENERATIVE MEMBRANE INTENDED TO BE USED AS TEMPORARY SUPPORT IN GUIDED TISSUE REGENERATION PROCEDURES, BOTH IN ORGANS AND TISSUES

Manufacturer
City
JOINVILLE
Country
BRAZIL
Address
AV. EDGAR NELSON MEISTER, 474 - DISTRITO INDUSTRIAL - 89219-501 –JOINVILLE - SC – BRAZIL
Product Owner
Name
DENTSCARE LTDA.
Country
BRAZIL
Authorized Representative
Address
REPUBLIC OF EL SALVADOR N34 399 AND IRELAND
Phone
2385228