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Amnioscope - ANVISA Registration 81094800009

Access comprehensive regulatory information for Amnioscope in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 81094800009 and manufactured by ORTOFEX INDÚSTRIA E COMÉRCIO DE APARELHOS MÉDICOS E ORTOPÉDICOS LTDA.-ME. The registration is held by ORTOFEX INDÚSTRIA E COMÉRCIO DE APARELHOS MÉDICOS E ORTOPÉDICOS LTDA.-ME with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 2 companies making the same product including MICROEM PRODUTOS MEDICOS LTDA., CIRUVET INDUSTRIA E COMERCIO LTDA EPP, and 2 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.

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81094800009
Registration Details
ANVISA Registration Number: 81094800009
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Device Details

AMNIOSCÓPIO MANUAL RSP HOSPITALAR
Risk Class I

Registration Details

81094800009

25351741918201416

19973704000179

Dates and Status

Mar 02, 2015

VIGENTE

09/18/2025 19:00:01

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