International safety notice
Sample Processor for Healthcare Diagnostics
Brazil / Anvisa · BRA · Mar 4, 2016
Key facts
| Title | Sample Processor for Healthcare Diagnostics |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Cobas p 512 Pre-Analytical System, records 10287411043 and 10287410844, risk class I, various series: 4700920; |
| Manufacturer | DETENTOR DO REGISTRO ROCHE DIAGNÓSTICA BRASIL LTDA ENDEREÇO AVENIDA ENGENHEIRO BILLINGS 1729 PRÉDIO 38 SÃO PAULOSP FABRICANTE ROCHE DIAGNOSTICS GMBH ENDEREÇO SANDHOFER STRASSE 116 68305ALEMANHA |
| Models | 4725345, 4727545, 4707431, 4707331, 4700920, 4707131, 4706831, 4725245, 4714441, 4732745, 4733045, 4706731 and 33 more |
| Date | Mar 4, 2016 |
| 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