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ANVISA registration 80835239003Active

Dry Powder Inhaler

ANVISA Registration Number: 80835239003COSMED INDUSTRIA DE COSMETICOS E MEDICAMENTOS S.A.PLASTIAPE S.P.A. ITALYRisk Class I
Verified
Device names
Technical name
Dry Powder Inhaler
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PT: Dispositivo para Inalação com Pó Seco
Commercial name
INALADOR MONODOSE MODELO 3
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Risk class
Class I
Registration details
Registration Number
80835239003
Process Number
25351048607201703
CNPJ
61082426000207
Company information
Registration Holder
COSMED INDUSTRIA DE COSMETICOS E MEDICAMENTOS S.A.
Manufacturer
PLASTIAPE S.P.A. ITALY
Manufacturing Country
Italy
PT: ITÁLIA
Dates and status
Publication Date
Feb 20, 2017
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Dry Powder Inhaler in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80835239003 and manufactured by PLASTIAPE S.P.A. ITALY. The registration is held by COSMED INDUSTRIA DE COSMETICOS E MEDICAMENTOS S.A. 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.