Retinoscope - ANVISA Registration 80011680077
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 80011680077 and manufactured by WELCH ALLYN INC.. The registration is held by WELCH ALLYN DO BRASIL, COMÉRCIO DE EQUIPAMENTOS MÉDICOS LTDA with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including KEELER LTD., CARL ZEISS MEDITEC INC. (DUBLIN-US), and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
Registration Details
80011680077
25351566332201222
03135603000199
Company Information
Dates and Status
Apr 22, 2013
VIGENTE
09/18/2025 19:00:01
Retinoscopio
RETINOSCÓPIO
SUZHOU KANGJIE MEDICAL INC.
80310280011
Dec 18, 2023
Retinoscopio
Retinoscópio Keeler
KEELER LTD.
80891620081
Feb 03, 2022
Retinoscopio
AUTOREFRATOR PLUSOPTIX
Plusoptix Gmbh
80548419006
Jan 21, 2021
Retinoscopio
Microscópio de Operação
TAKAGI SEIKO CO., LTD
80170800015
Sep 05, 2019
Retinoscopio
CLARUS
CARL ZEISS MEDITEC INC. (DUBLIN-US)
10332030108
Apr 23, 2018

