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BIONGRAFT BARRIER MEMBRANE 20x25 - ARCSA Registration 04e98215f5a1ff97ea685b7cbcd15d34

Access comprehensive regulatory information for BIONGRAFT BARRIER MEMBRANE 20x25 in the Ecuador medical device market through Pure Global AI's free database. This IV medical device is registered under ARCSA ID 04e98215f5a1ff97ea685b7cbcd15d34 and manufactured by BONEGRAFT BIOLOGICAL MATERIALS SAN. VE TIC. A.S.. The device was registered on August 14, 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
04e98215f5a1ff97ea685b7cbcd15d34
BIONGRAFT BARRIER MEMBRANE 20x25
ARCSA ID: 04e98215f5a1ff97ea685b7cbcd15d34
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Device Classification
Risk Class
IV
Product Type
Invasive
Brand Name
BIONGRAFT
Commercial Name
BONE GRAFTS
Sterilization Method
GAMMA RADIATION
Registration Information
Analysis ID
04e98215f5a1ff97ea685b7cbcd15d34
Registration Date
August 14, 2022
Expiration Date
August 14, 2027
Creation Date
August 14, 2022
Product Use

DESIGNED AS A BONE SUBSTITUTE FOR SUPPORTING THE FORMATION OF BONE TISSUE IN BONE DEFECTS

Manufacturer
City
IZMIR
Country
TURKEY
Address
7410 SOK. NO: 8 KEMALPASA MAH. PINARBASI BORNOVA
Product Owner
Name
CRUVAL, S.L
Country
SPAIN
Authorized Representative
Address
MANUELA SAENZ N34-259 AND ABELARDO MONCAYO
Phone
2442768