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ANVISA registration 80350200002Active

Dry Powder Inhaler

ANVISA Registration Number: 80350200002QUALITEC INDUSTRIA E COMERCIO DE PLASTICOS LTDAQUALITEC INDUSTRIA E COMERCIO DE PLASTICOS LTDARisk Class I
Verified
Device names
Technical name
Dry Powder Inhaler
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PT: Dispositivo para Inalação com Pó Seco
Commercial name
INALADOR CDM
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Risk class
Class I
Registration details
Registration Number
80350200002
Process Number
25351223026201115
CNPJ
00890648000180
Company information
Registration Holder
QUALITEC INDUSTRIA E COMERCIO DE PLASTICOS LTDA
Manufacturer
QUALITEC INDUSTRIA E COMERCIO DE PLASTICOS LTDA
Manufacturing Country
Brazil
PT: BRASIL
Dates and status
Publication Date
Jun 13, 2011
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 80350200002 and manufactured by QUALITEC INDUSTRIA E COMERCIO DE PLASTICOS LTDA. The registration is held by QUALITEC INDUSTRIA E COMERCIO DE PLASTICOS LTDA 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.