GENERAL PURPOSE GUIDE WIRE, NON-VASCULAR - ANVISA Registration 10212990217

Access comprehensive regulatory information for GENERAL PURPOSE GUIDE WIRE, NON-VASCULAR in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10212990217 and manufactured by COOK ENDOSCOPY. The registration is held by E TAMUSSINO E CIA LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including BOSTON SCIENTIFIC CORPORATION, BLUE NEEM MEDICAL DEVICES PRIVATE LIMITED, 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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10212990217
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Registration Details
ANVISA Registration Number: 10212990217
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

FIO GUIA PARA CÂNULA DILATADORA SAVARY-GILLIARD
Risk Class II

Registration Details

10212990217

25351148423200735

33100082000103

Company Information

COOK ENDOSCOPY
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Aug 27, 2007

VIGENTE

09/18/2025 19:00:01

FIO GUIA PARA CÂNULA DILATADORA SAVARY-GILLIARD
Risk Class II

Registration Details

10212990217

25351148423200735

33100082000103

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Aug 27, 2007

VIGENTE

09/18/2025 19:00:01