INTERFERON A/B/Y - ANVISA Registration 10322250078
Access comprehensive regulatory information for INTERFERON A/B/Y in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10322250078 and manufactured by QIAGEN. The registration is held by QIAGEN BIOTECNOLOGIA 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, 1 companies making the same product including QIAGEN, and 1 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
10322250078
25351202350201731
01334250000120
Company Information
Dates and Status
Oct 31, 2017
VIGENTE
09/18/2025 19:00:01
ANTI-INTRINSIC FACTOR ANTIBODY
ANTI FATOR INTRINSECO ELISA
ORGENTEC DIAGNOSTIKA GMBH
10300390789
Jul 08, 2019
ANTI-INTRINSIC FACTOR ANTIBODY
EliA Intrinsic Factor Well
PHADIA AB
80254180382
Feb 18, 2021
ANTI-INTRINSIC FACTOR ANTIBODY
ACCESS INTRINSIC FACTOR Ab QC
BECKMAN COULTER, INC.
10033120546
Jun 25, 2007
IMMUNOGLOBULIN A
IgA Saliva ELISA
LDN LABOR DIAGNOSTIKA NORD GMBH & CO.
80464810527
Sep 04, 2017
IMMUNOGLOBULIN A
ELIA IGA CONJUGATE 200
PHADIA AB
80254180137
Jul 11, 2011