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ANVISA registration 80978879001Active

Dry Powder Inhaler

ANVISA Registration Number: 80978879001CIPLA BRASIL IMPORTADORA E DISTRIBUIDORA DE MEDICAMENTOS LTDACIPLA LIMITEDRisk Class II
Verified
Device names
Technical name
Dry Powder Inhaler
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PT: Dispositivo para Inalação com Pó Seco
Commercial name
Wakeeta®
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Risk class
Class II
Registration details
Registration Number
80978879001
Process Number
25351461387202401
CNPJ
18268051000164
Company information
Registration Holder
CIPLA BRASIL IMPORTADORA E DISTRIBUIDORA DE MEDICAMENTOS LTDA
Manufacturer
CIPLA LIMITED
Manufacturing Country
India
PT: ÍNDIA
Dates and status
Publication Date
Mar 10, 2025
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 II medical device is registered under ANVISA number 80978879001 and manufactured by CIPLA LIMITED. The registration is held by CIPLA BRASIL IMPORTADORA E DISTRIBUIDORA DE MEDICAMENTOS 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.