International safety notice
RUBELLA VIRUS
Brazil / Anvisa · BRA · Nov 21, 2014
Key facts
| Title | RUBELLA VIRUS |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | VITROS* IMMUNODIAGNOSTIC REAGENT KIT FOR RUBELLA IgM - registration 80145901047. Lots 0740 and 0751. See Appendix 1 Distribution List |
| Manufacturer | DETENTOR DO REGISTRO NO BRASIL JOHNSON JOHNSON DO BRASIL IND E COM DE PROD PARA SAÚDE LTDA CNPJ 54516661000101 ENDEREÇO RUA GERIVATIBA NO 207 SÃO PAULO SÃO PAULO TELEFONE 12 3932 1659 FABRICANTE ORTHOCLINICAL DIAGNOSTICS 50100 HOLMERS FARM WAY HIGH WYCOMBE BUCKINGHAMSHIRE HP 12 4DP REINO UNIDO |
| Models | 80145901047 |
| Date | Nov 21, 2014 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1