ESTRADIOL - ANVISA Registration 80146501208
Access comprehensive regulatory information for ESTRADIOL in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80146501208 and manufactured by ABBOTT IRELAND DIAGNOSTICS DIVISION. The registration is held by ABBOTT LABORATORIOS 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 SIEMENS HEALTHCARE DIAGNOSTICS INC., ROCHE DIAGNOSTICS GMBH, 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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Registration Details
80146501208
25351242271200413
56998701000116
Company Information
Dates and Status
Feb 18, 2005
VIGENTE
09/18/2025 19:00:01
PROGESTERONE
ARCHITECT PROGESTERONE CONTROLS
ABBOTT LABORATORIES
10055310996
Oct 09, 2000
PROGESTERONE
ARCHITECT PROGESTERONE CONTROLS
ABBOTT IRELAND DIAGNOSTICS DIVISION
10055310996
Oct 09, 2000
TESTOSTERONE
ARCHITECT 2nd Generation Testosterone Controls
ABBOTT GMBH
80146501787
Jun 25, 2012
PROLACTIN
ARCHITECT PROLACTIN CONTROLS
ABBOTT IRELAND DIAGNOSTICS DIVISION
10055311010
Oct 09, 2000
PROLACTIN
ARCHITECT PROLACTIN CONTROLS
ABBOTT LABORATORIES
10055311010
Oct 09, 2000
SIEMENS HEALTHCARE DIAGNOSTICS INC.• United States of America
ROCHE DIAGNOSTICS GMBH• Germany
SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED• United Kingdom
SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD• China
LDN LABOR DIAGNOSTIKA NORD GMBH & CO.• Germany
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