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TROPONIN - ANVISA Registration 10345162200

Access comprehensive regulatory information for TROPONIN in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10345162200 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD. The registration is held by SIEMENS HEALTHCARE DIAGNÓSTICOS LTDA with validity until Feb 26, 2028.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including ROCHE DIAGNOSTICS GMBH, BODITECH MED INC., 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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10345162200
2 Related Devices
Registration Details
ANVISA Registration Number: 10345162200
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Related Devices (2)

TROPONINA I TURBO IMMULITE / IMMULITE 1000
Risk Class III

Registration Details

10345162200

25351683386201789

01449930000190

Company Information

United Kingdom
PT: REINO UNIDO

Dates and Status

Feb 26, 2018

26/02/2028

09/18/2025 19:00:01

TROPONINA I TURBO IMMULITE / IMMULITE 1000
Risk Class III

Registration Details

10345162200

25351683386201789

01449930000190

Company Information

Dates and Status

Feb 26, 2018

26/02/2028

09/18/2025 19:00:01