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Disposable Amniotic Membrane Rupturer - ANVISA Registration 80269339004

Access comprehensive regulatory information for Disposable Amniotic Membrane Rupturer in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80269339004 and manufactured by BRIGGS MEDICAL SERVICE COMPANY. The registration is held by HOSPILINE COMÉRCIO E DISTRIBUIÇÃO DE PRODUTOS MÉDICOS HOSPITALARES 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 KYJ Medical Products Co., Ltd., KOLPLAST CI LTDA, 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.

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80269339004
Registration Details
ANVISA Registration Number: 80269339004
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Device Details

AMNIHOOK ROMPEDOR DE MEMBRANA AMNIÓTICA DESCARTÁVEL
Risk Class II

Registration Details

80269339004

25351069135201111

07424092000186

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jun 13, 2011

VIGENTE

09/18/2025 19:00:01