Endoscopic Forceps - ANVISA Registration 81263810002

Access comprehensive regulatory information for Endoscopic Forceps in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 81263810002 and manufactured by G-FLEX AMÉRICA LATINA - INDÚSTRIA DE PRODUTOS MANUFATURADOS LTDA. The registration is held by G-FLEX AMÉRICA LATINA - INDÚSTRIA DE PRODUTOS MANUFATURADOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME, RICHARD WOLF GMBH, 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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81263810002
Registration Details
ANVISA Registration Number: 81263810002
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

PINÇA FLEXÍVEL REUTILIZÁVEL PARA ENDOSCOPIA
Risk Class I

Registration Details

81263810002

25351571378201542

19865312000196

Dates and Status

Apr 25, 2016

VIGENTE

09/18/2025 19:00:01