PROGESTERONE - ANVISA Registration 10345160655

Access comprehensive regulatory information for PROGESTERONE in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10345160655 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED. The registration is held by SIEMENS HEALTHCARE DIAGNÓSTICOS LTDA with validity until currently active (VIGENTE).

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 ROCHE DIAGNOSTICS GMBH, ABBOTT LABORATORIES, 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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10345160655
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Registration Details
ANVISA Registration Number: 10345160655
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

PROGESTERONA IMMULITE/IMMULITE1000
Risk Class II

Registration Details

10345160655

25351022662200847

01449930000190

Company Information

United Kingdom
PT: REINO UNIDO

Dates and Status

Apr 22, 2008

VIGENTE

09/18/2025 19:00:01

PROGESTERONA IMMULITE/IMMULITE1000
Risk Class II

Registration Details

10345160655

25351022662200847

01449930000190

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Apr 22, 2008

VIGENTE

09/18/2025 19:00:01