Instrument Kit - ANVISA Registration 10392060059

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 10392060059 and manufactured by ORTHOFIX SRL. The registration is held by ORTHOFIX DO BRASIL 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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10392060059
Registration Details
ANVISA Registration Number: 10392060059
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

FRESA FLEXÍVEL ORTHOFIX
Risk Class I

Registration Details

10392060059

25351878459200806

02690906000100

Company Information

ORTHOFIX SRL
Italy
PT: ITÁLIA

Dates and Status

Nov 23, 2009

VIGENTE

09/18/2025 19:00:01