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ANVISA registration 81431610003Valid until Jul 09, 2027

Disc replacement interbody spacing device

ANVISA Registration Number: 81431610003Medicine Health Solution ltda meNEURO FRANCE IMPLANTSRisk Class III
Verified
Device names
Technical name
Disc replacement interbody spacing device
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PT: Dispositivo de espaçamento intersomático de substituição discal
Commercial name
CAGE INTERSOMÁTICO NÃO EXPANSIVO - PEEK
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Risk class
Class III
Registration details
Registration Number
81431610003
Process Number
25351314171201752
CNPJ
22337493000192
Company information
Registration Holder
Medicine Health Solution ltda me
Manufacturer
NEURO FRANCE IMPLANTS
Manufacturing Country
France
PT: FRANÇA
Dates and status
Publication Date
Sep 11, 2017
Validity
09/07/2027
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Disc replacement interbody spacing device in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81431610003 and manufactured by NEURO FRANCE IMPLANTS. The registration is held by Medicine Health Solution ltda me with validity until Jul 09, 2027.

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.