ESTRADIOL - ANVISA Registration 80146501210
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 80146501210 and manufactured by ABBOTT IRELAND DIAGNOSTIC 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
80146501210
25351242378200461
56998701000116
Company Information
Dates and Status
Feb 18, 2005
VIGENTE
09/18/2025 19:00:01
ESTRADIOL
ARCHITECT ESTRADIOL CONTROLS
ABBOTT IRELAND DIAGNOSTICS DIVISION
80146501208
Feb 18, 2005
PROGESTERONE
ARCHITECT PROGESTERONE REAGENTS
ABBOTT IRELAND DIAGNOSTIC DIVISION
10055311012
Oct 09, 2000
C-PEPTIDE
ARCHITECT C PEPTIDE REAGENTS
ABBOTT LABORATORIES
80146501561
Nov 10, 2008
C-PEPTIDE
ARCHITECT C PEPTIDE REAGENTS
ABBOTT GMBH
80146501561
Nov 10, 2008
FOLATE
ARCHITECT FOLATE RAGENT KIT - ARCHITECT FOLATO REAGENTE
ABBOTT IRELAND DIAGNOSTIC DIVISION
80146501394
Dec 11, 2006
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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