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Instrument Kit - ANVISA Registration 80005430240

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 80005430240 and manufactured by STRYKER TRAUMA GMBH (SCHONKIRCHEN). The registration is held by STRYKER 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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80005430240
2 Related Devices
Registration Details
ANVISA Registration Number: 80005430240
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Related Devices (2)

INSTRUMENTAL T2 STRYKER TRAUMA
Risk Class I

Registration Details

80005430240

25351010139201010

02966317000102

Company Information

Germany
PT: ALEMANHA

Dates and Status

Sep 26, 2011

VIGENTE

09/18/2025 19:00:01

INSTRUMENTAL T2 STRYKER TRAUMA
Risk Class I

Registration Details

80005430240

25351010139201010

02966317000102

Company Information

STRYKER GMBH
Switzerland
PT: SUรร‡A

Dates and Status

Sep 26, 2011

VIGENTE

09/18/2025 19:00:01