CERULOPLASMIN - ANVISA Registration 10345162354
Access comprehensive regulatory information for CERULOPLASMIN in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10345162354 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS, INC. - EUA. The registration is held by SIEMENS HEALTHCARE DIAGNÓSTICOS LTDA 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 ROCHE DIAGNOSTICS GMBH, SENTINEL CH. SPA, 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
10345162354
25351317331201945
01449930000190
Company Information
Dates and Status
Apr 06, 2020
VIGENTE
09/18/2025 19:00:01
CERULOPLASMINA
Ceruloplasmina
VYTTRA DIAGNOSTICOS S.A.
81692610214
Dec 10, 2020
CERULOPLASMINA
Alinity c Ceruloplasmin Reagent Kit
SENTINEL CH. SPA
80146502245
Feb 26, 2020
CERULOPLASMINA
CERU (Ceruloplasmin)_cobas c
ROCHE DIAGNOSTICS GMBH
10287411469
Jan 27, 2020
CERULOPLASMINA
Optilite Caeruloplasmin Kit
THE BINDING SITE GROUP LTD
81357320027
Nov 20, 2017
CERULOPLASMINA
Ceruloplasmin Calibrator Turbitest AA
WIENER LABORATÓRIOS S.A.I.C.
10268590324
Mar 02, 2015