Guide Wire - ANVISA Registration 10392060049

Access comprehensive regulatory information for Guide Wire in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10392060049 and manufactured by manufacturer not specified. The registration is held by ORTHOFIX DO BRASIL LTDA. with validity until Jan 21, 2028.

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 E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME, SP MEDICAL A/S, 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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10392060049
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Registration Details
ANVISA Registration Number: 10392060049
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

FIO KIRSCHNER X-WIRE ORTHOFIX
Risk Class III

Registration Details

10392060049

25351384244200689

02690906000100

Company Information

Dates and Status

Jan 21, 2008

21/01/2028

09/18/2025 19:00:01

FIO KIRSCHNER X-WIRE ORTHOFIX
Risk Class III

Registration Details

10392060049

25351384244200689

02690906000100

Company Information

ORTHOFIX SRL
Italy
PT: ITÁLIA

Dates and Status

Jan 21, 2008

21/01/2028

09/18/2025 19:00:01