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ANVISA registration 81065910004Valid until Oct 19, 2030

BONE GRAFT AND ASSOCIATED DEVICES

ANVISA Registration Number: 81065910004ENTERFIX IMPORTACAO E COMERCIO DE PRODUTOS MEDICO-HOSPITALARES LTDANORAKERRisk Class IV
Device names
Technical name
BONE GRAFT AND ASSOCIATED DEVICES
PT: ENXERTO PARA OSSOS E DISPOSITIVOS ASSOCIADOS
Commercial name
BIO-LOGIC GLASS PUTTY
Risk class
Class IV
Registration details
Registration Number
81065910004
Process Number
25351658218201917
CNPJ
18312747000140
Company information
Manufacturer
NORAKER
Manufacturing Country
France
PT: FRANÇA
Dates and status
Publication Date
Oct 19, 2020
Validity
19/10/2030
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 81065910004 and manufactured by NORAKER. The registration is held by ENTERFIX IMPORTACAO E COMERCIO DE PRODUTOS MEDICO-HOSPITALARES LTDA with validity until Oct 19, 2030.

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.