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ANVISA registration 80117581284Active

Retinoscope

ANVISA Registration Number: 80117581284EMERGO BRAZIL IMPORT IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS HOSPITALARES LTDAKEELER LTD.Risk Class I
Verified
Device names
Technical name
Retinoscope
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PT: Retinoscopio
Commercial name
Retinoscópio Keeler
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Risk class
Class I
Registration details
Registration Number
80117581284
Process Number
25351057941202611
CNPJ
04967408000198
Company information
Registration Holder
EMERGO BRAZIL IMPORT IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS HOSPITALARES LTDA
Manufacturer
KEELER LTD.
Manufacturing Country
United Kingdom
PT: REINO UNIDO
Dates and status
Publication Date
Apr 27, 2026
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Retinoscope in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80117581284 and manufactured by KEELER LTD.. The registration is held by EMERGO BRAZIL IMPORT IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS HOSPITALARES 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.