HERPES VIRUS (HHV 3) - VARICELLA ZOSTER - ANVISA Registration 81905510039
Access comprehensive regulatory information for HERPES VIRUS (HHV 3) - VARICELLA ZOSTER in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81905510039 and manufactured by manufacturer not specified. The registration is held by GMRB COMÉRCIO DE PRODUTOS MÉDICOS E DIAGNÓSTICOS LTDA with validity until Feb 17, 2034.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including ORGENTEC DIAGNOSTIKA GMBH, DIASORIN ITALIA S.P.A., 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
81905510039
25351243487202288
34255136000164
Company Information
Dates and Status
Nov 28, 2022
17/02/2034
09/18/2025 19:00:01
HERPES VÍRUS (HHV 3) - VARICELLA ZOSTER
Família LIAISON® VZV IgG HT
Not specified
10339840558
Jan 13, 2025
HERPES VÍRUS (HHV 3) - VARICELLA ZOSTER
Família LIAISON® VZV IgG HT
DIASORIN ITALIA S.P.A.
10339840558
Jan 13, 2025
HERPES VÍRUS (HHV 3) - VARICELLA ZOSTER
AltoStar® VZV PCR Kit 1.5
ALTONA DIAGNOSTICS GMBH
81752180027
Oct 23, 2023
HERPES VÍRUS (HHV 3) - VARICELLA ZOSTER
AltoStar® VZV PCR Kit 1.5
Not specified
81752180027
Oct 23, 2023
HERPES VÍRUS (HHV 3) - VARICELLA ZOSTER
SERION ELISA classic Varicella-Zoster Virus IgM
Not specified
81905510036
Nov 28, 2022

