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ANVISA registration 10334789008Active

Esophageal Dilators

ANVISA Registration Number: 10334789008G.F.E. DO BRASIL LTDA.DIVERSATEK HEALTHCARE INC.Risk Class I
Verified
Device names
Technical name
Esophageal Dilators
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PT: Dilatadores Esofagicos
Commercial name
BUGIA DILATADORA - M-FLEX
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Risk class
Class I
Registration details
Registration Number
10334789008
Process Number
25351263601202458
CNPJ
55126981000100
Company information
Registration Holder
G.F.E. DO BRASIL LTDA.
Manufacturer
DIVERSATEK HEALTHCARE INC.
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
May 20, 2024
Status
Active
Official value: VIGENTE
About this record

Access comprehensive regulatory information for Esophageal Dilators in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10334789008 and manufactured by DIVERSATEK HEALTHCARE INC.. The registration is held by G.F.E. DO BRASIL 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.