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NANOSYNT - ARCSA Registration 119c722101e53e8dc100bc2a62cd4ce6

Access comprehensive regulatory information for NANOSYNT in the Ecuador medical device market through Pure Global AI's free database. This IV medical device is registered under ARCSA ID 119c722101e53e8dc100bc2a62cd4ce6 and manufactured by DENTSCARE LTDA.. The device was registered on November 20, 2019.

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
119c722101e53e8dc100bc2a62cd4ce6
NANOSYNT
ARCSA ID: 119c722101e53e8dc100bc2a62cd4ce6
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Device Classification
Risk Class
IV
Product Type
Invasive
Brand Name
FGM
Commercial Name
Grafts, Bones, Synthetic
Sterilization Method
GAMMA RADIATION
Registration Information
Analysis ID
119c722101e53e8dc100bc2a62cd4ce6
Registration Date
November 20, 2019
Expiration Date
November 20, 2024
Creation Date
July 13, 2022
Product Use

IT IS AN IMPLANTABLE BIOMATERIAL OF OSTEOCONDUCTIVE ACTION, BEING REABSORBED AND REPLACED BY LIVING BONE TISSUE DURING BONE REMODELING.

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