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ANVISA registration 81704060018Valid until Mar 16, 2036

BONE GRAFT AND ASSOCIATED DEVICES

ANVISA Registration Number: 81704060018EVO MEDICINA ESPECIALIZADA LTDABONEGRAFT BIYOLOJIK MALZEMELER SANAYI VE TICARET A.SRisk Class IV
Verified
Device names
Technical name
BONE GRAFT AND ASSOCIATED DEVICES
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PT: ENXERTO PARA OSSOS E DISPOSITIVOS ASSOCIADOS
Commercial name
BONEGRAFT PUTTY
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Risk class
Class IV
Registration details
Registration Number
81704060018
Process Number
25351429357202401
CNPJ
14021783000102
Company information
Registration Holder
EVO MEDICINA ESPECIALIZADA LTDA
Manufacturer
BONEGRAFT BIYOLOJIK MALZEMELER SANAYI VE TICARET A.S
Manufacturing Country
Türkiye
PT: TURQUIA
Dates and status
Publication Date
Mar 16, 2026
Validity
16/03/2036
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for BONE GRAFT AND ASSOCIATED DEVICES in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 81704060018 and manufactured by BONEGRAFT BIYOLOJIK MALZEMELER SANAYI VE TICARET A.S. The registration is held by EVO MEDICINA ESPECIALIZADA LTDA with validity until Mar 16, 2036.

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.