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ANVISA registration 10247530110Valid until Jul 29, 2028

Disc replacement interbody spacing device

ANVISA Registration Number: 10247530110IMPLAMED-IMPLANTES ESPECIALIZADOS COM IMPOR E EXPOR LTDAORTHOFIX INC.Risk 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
FAMÍLIA DE CAGES ESTÉREIS ORTHOFIX
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Risk class
Class III
Registration details
Registration Number
10247530110
Process Number
25351336234201231
CNPJ
57146607000100
Company information
Registration Holder
IMPLAMED-IMPLANTES ESPECIALIZADOS COM IMPOR E EXPOR LTDA
Manufacturer
ORTHOFIX INC.
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Jul 29, 2013
Validity
29/07/2028
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 10247530110 and manufactured by ORTHOFIX INC.. The registration is held by IMPLAMED-IMPLANTES ESPECIALIZADOS COM IMPOR E EXPOR LTDA with validity until Jul 29, 2028.

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.