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ANVISA registration 80102512637Valid until Mar 15, 2031

BONE GRAFT AND ASSOCIATED DEVICES

ANVISA Registration Number: 80102512637VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDAPURGO BIOLOGICS INC.Risk 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
THE GRAFT
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Risk class
Class IV
Registration details
Registration Number
80102512637
Process Number
25351363198202032
CNPJ
04718143000194
Company information
Registration Holder
VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA
Manufacturer
PURGO BIOLOGICS INC.
Manufacturing Country
South Korea
PT: CORÉIA DO SUL
Dates and status
Publication Date
Mar 15, 2021
Validity
15/03/2031
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 80102512637 and manufactured by PURGO BIOLOGICS INC.. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Mar 15, 2031.

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.