ANVISA registration 81244549003Active

Dry Powder Inhaler

Name: Dry Powder Inhaler — ANVISA registration 81244549003
Creator: MANNKIND CORPORATION
Keywords: Dry Powder Inhaler, Dispositivo para Inalação com Pó Seco, Inalador AFREZZA, 81244549003, Risk Class I, ANVISA registration

ANVISA Registration Number: 81244549003BIOMM SAMANNKIND CORPORATIONRisk Class I

Verified

Device names

Technical name: Dry Powder Inhaler
Commercial name: Inalador AFREZZA
Risk class: Class I

Registration details

Registration Number: 81244549003
Process Number: 25351187868201893
CNPJ: 04752991000110

Company information

Registration Holder: BIOMM SA
Manufacturer: MANNKIND CORPORATION
Manufacturing Country: United States

Dates and status

Publication Date: Apr 30, 2018
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 81244549003 and manufactured by MANNKIND CORPORATION. The registration is held by BIOMM SA 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.