International safety notice
COBAS P PRE-ANALYTIC FAMILY - SAMPLE PROCESSOR FOR HEALTH DIAGNOSIS
Brazil / Anvisa · BRA · Oct 1, 2015
Key facts
| Title | COBAS P PRE-ANALYTIC FAMILY - SAMPLE PROCESSOR FOR HEALTH DIAGNOSIS |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Bulk Loader (BLM), module integral to the Cobas p 512/612 equipment; |
| Manufacturer | DETENTOR DO REGISTRO ROCHE DIAGNÓSTICA BRASIL LTDA CNPJ 302803580001 86 ENDEREÇO AVENIDA ENGENHEIRO BILLINGS 1729 PRÉDIO 38 SÃO PAULO FABRICANTE ROCHE DIAGNOSTICS GMBH ENDEREÇO SANDHOFER STRASSE 116 68305 ALEMANHA |
| Models | 7501921, 7501821, 7501721, 10287411043, 7502021 |
| Date | Oct 1, 2015 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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