VANCOMYCIN - ANVISA Registration 80254180384
Access comprehensive regulatory information for VANCOMYCIN in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80254180384 and manufactured by manufacturer not specified. The registration is held by PHADIA DIAGNOSTICOS LTDA with validity until Mar 15, 2031.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 3 companies making the same product including CEPHEID AB, ORTHO CLINICAL 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.
Related Devices (2)
Registration Details
80254180384
25351012057202135
04930429000139
Company Information
Dates and Status
Mar 15, 2021
15/03/2031
09/18/2025 19:00:01
VANCOMICINA
Xpert VanA/VanB
Not specified
81062710060
Sep 15, 2025
VANCOMICINA
Xpert VanA/VanB
CEPHEID AB
81062710060
Sep 15, 2025
VANCOMICINA
Famรญlia VITROS Chemistry Products VANC Reagent and Calibrator
ORTHO CLINICAL DIAGNOSTICS, INC
81246986911
Jun 09, 2025
VANCOMICINA
Famรญlia VITROS Chemistry Products VANC Reagent and Calibrator
Not specified
81246986911
Jun 09, 2025
VANCOMICINA
Vancomycin resistance for BD Max System
Not specified
10033430829
Jun 17, 2021

