AUTOIMMUNE HEPATITIS (AIH) ANTIBODY - ANVISA Registration 10300390701
Access comprehensive regulatory information for AUTOIMMUNE HEPATITIS (AIH) ANTIBODY in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10300390701 and manufactured by ORGENTEC DIAGNOSTIKA GMBH. The registration is held by VYTTRA DIAGNOSTICOS S.A. with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including ORGENTEC DIAGNOSTIKA GMBH, INOVA DIAGNOSTICS, 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.
Device Details
Registration Details
10300390701
25351251658201947
00904728000148
Company Information
Dates and Status
May 20, 2019
VIGENTE
09/18/2025 19:00:01
ANTICORPO PARA HEPATITE AUTOIMUNE (HAI)
Famรญlia QUANTA Flash LKM-1
INOVA DIAGNOSTICS, INC.
80003610580
Aug 10, 2020
ANTICORPO PARA HEPATITE AUTOIMUNE (HAI)
Anti-LKM-1
ORGENTEC DIAGNOSTIKA GMBH
10300390509
May 20, 2019
ANTICORPO PARA HEPATITE AUTOIMUNE (HAI)
Anti-SLA
ORGENTEC DIAGNOSTIKA GMBH
10300390607
May 20, 2019
ANTICORPO PARA HEPATITE AUTOIMUNE (HAI)
LIVER-9-LINE 2nd Generation
ORGENTEC DIAGNOSTIKA GMBH
10300390669
May 20, 2019
ANTICORPO PARA HEPATITE AUTOIMUNE (HAI)
ANTICORPOS ANTI-MUSCULO LISO (ASMA)
BIOSYSTEMS S.A.
10300390082
Dec 17, 2018

