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ANVISA registration 10306840218Valid until Jun 29, 2036

ANCHOR

ANVISA Registration Number: 10306840218PROMEDON DO BRASIL PRODUTOS MEDICO HOSPITALARES LTDAPROMEDON S.A.Risk Class III
Verified
Device names
Technical name
ANCHOR
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PT: ÂNCORA
Commercial name
Âncoras de PEEK para tenodese
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Risk class
Class III
Registration details
Registration Number
10306840218
Process Number
25351463032202449
CNPJ
00028682000140
Company information
Registration Holder
PROMEDON DO BRASIL PRODUTOS MEDICO HOSPITALARES LTDA
Manufacturer
PROMEDON S.A.
Manufacturing Country
Argentina
PT: ARGENTINA
Dates and status
Publication Date
Jun 29, 2026
Validity
29/06/2036
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for ANCHOR in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10306840218 and manufactured by PROMEDON S.A.. The registration is held by PROMEDON DO BRASIL PRODUTOS MEDICO HOSPITALARES LTDA with validity until Jun 29, 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.