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ANVISA registration 80825800003Active

Humidifier

ANVISA Registration Number: 80825800003RESPIROX COMÉRCIO DE OXIGÊNIO LTDA - EPPSALTER LABS DE MEXICO S.A. DE C.V.Risk Class II
Verified
Device names
Technical name
Humidifier
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PT: Umidificador
Commercial name
UMIDIFICADOR SALTER LABS
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Risk class
Class II
Registration details
Registration Number
80825800003
Process Number
25351537438201397
CNPJ
74663972000100
Company information
Registration Holder
RESPIROX COMÉRCIO DE OXIGÊNIO LTDA - EPP
Manufacturer
SALTER LABS DE MEXICO S.A. DE C.V.
Manufacturing Country
Mexico
PT: MÉXICO
Dates and status
Publication Date
Oct 21, 2013
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Humidifier in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80825800003 and manufactured by SALTER LABS DE MEXICO S.A. DE C.V.. The registration is held by RESPIROX COMÉRCIO DE OXIGÊNIO LTDA - EPP with validity until currently active (VIGENTE).

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.