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ANVISA registration 80891620082Active

Otoscope

ANVISA Registration Number: 80891620082Halma Saúde e Ótica do Brasil Importação Exportação e Distribuição LtdaKEELER LTD.Risk Class I
Verified
Device names
Technical name
Otoscope
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PT: Otoscopio
Commercial name
Otoscópio Keeler
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Risk class
Class I
Registration details
Registration Number
80891620082
Process Number
25351033789202240
CNPJ
13640053000119
Company information
Registration Holder
Halma Saúde e Ótica do Brasil Importação Exportação e Distribuição Ltda
Manufacturer
KEELER LTD.
Manufacturing Country
United Kingdom
PT: REINO UNIDO
Dates and status
Publication Date
Feb 03, 2022
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Otoscope in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80891620082 and manufactured by KEELER LTD.. The registration is held by Halma Saúde e Ótica do Brasil Importação Exportação e Distribuição 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.