Instrument Kit - ANVISA Registration 80012450018

Access comprehensive regulatory information for Instrument Kit in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80012450018 and manufactured by GREATBATCH MEDICAL SA. The registration is held by BIOSINTESE HOSPITALAR 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 MARDEN MEDICAL LTDA, LIMA CORPORATE S.P.A, 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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80012450018
Registration Details
ANVISA Registration Number: 80012450018
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

KIT DE FRESAS INTRA-MODULARES FLEXÍVEIS DE NITINOL
Risk Class I

Registration Details

80012450018

25351140156201249

01086229000153

Company Information

Switzerland
PT: SUÍÇA

Dates and Status

Jul 23, 2012

VIGENTE

09/18/2025 19:00:01