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Instrument Kit - ANVISA Registration 10392069010

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 10392069010 and manufactured by ORTHOFIX INC.. The registration is held by ORTHOFIX DO BRASIL LTDA. with validity until currently active (VIGENTE).

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 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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10392069010
2 Related Devices
Registration Details
ANVISA Registration Number: 10392069010
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Related Devices (2)

KIT INSTRUMENTAL PARA PLACAS IMPLANTÁVEIS ORTHOFIX
Risk Class I

Registration Details

10392069010

25351447140201218

02690906000100

Company Information

ORTHOFIX INC.
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jun 24, 2013

VIGENTE

09/18/2025 19:00:01

KIT INSTRUMENTAL PARA PLACAS IMPLANTÁVEIS ORTHOFIX
Risk Class I

Registration Details

10392069010

25351447140201218

02690906000100

Company Information

ORTHOFIX SRL
Italy
PT: ITÁLIA

Dates and Status

Jun 24, 2013

VIGENTE

09/18/2025 19:00:01