Bipolar Forceps - ANVISA Registration 80071910120

Access comprehensive regulatory information for Bipolar Forceps in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80071910120 and manufactured by OSTEOMED S.A. The registration is held by OSTEOMED S.A with validity until Sep 16, 2034.

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 euro parts brasil industria e comercio de instrumental cirurgico ltda, TECNO INSTRUMENTS (PVT) LTD., 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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80071910120
Registration Details
ANVISA Registration Number: 80071910120
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

Cânula Bipolar para Endoscopia Vert-FLEX
Risk Class IV

Registration Details

80071910120

25351381378202420

00638390000120

Company Information

OSTEOMED S.A
Brazil
PT: BRASIL

Dates and Status

Sep 16, 2024

16/09/2034

09/18/2025 19:00:01