RUBELLA VIRUS
ANVISA Registration Number: 81246986918ORTHO CLINICAL DIAGNÓSTICS DO BRASIL PRODUTOS PARA SAÚDE LTDAORTHO CLINICAL DIAGNOSTICSRisk Class III
Device names
- Commercial name
- Família VITROS Immunodiagnostic Products Rubella IgM Reagent Pack and Calibrator
- Risk class
- Class III
Registration details
- Registration Number
- 81246986918
- Process Number
- 25351014851202628
- CNPJ
- 21921393000146
Company information
- Registration Holder
- ORTHO CLINICAL DIAGNÓSTICS DO BRASIL PRODUTOS PARA SAÚDE LTDA
- Manufacturer
- ORTHO CLINICAL DIAGNOSTICS
- Manufacturing Country
- United Kingdom
PT: REINO UNIDO
Dates and status
- Publication Date
- Apr 22, 2026
- Validity
- 22/04/2036
- Last Updated
- 08/18/2026 19:00:00
About this record
Access comprehensive regulatory information for RUBELLA VIRUS in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81246986918 and manufactured by ORTHO CLINICAL DIAGNOSTICS. The registration is held by ORTHO CLINICAL DIAGNÓSTICS DO BRASIL PRODUTOS PARA SAÚDE LTDA with validity until Apr 22, 2036.
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