International safety notice
Analizador Cobas 6500 (Plataforma unida: cobas u 701 + cobas u 601) y Analizador Cobas u 701 (referencia 06390501)
Spain / AEMPS · ESP · Jul 8, 2021
Key facts
| Title | Analizador Cobas 6500 (Plataforma unida: cobas u 701 + cobas u 601) y Analizador Cobas u 701 (referencia 06390501) |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Analizador Cobas 6500 (Plataforma unida: cobas u 701 + cobas u 601) y Analizador Cobas u 701 (referencia 06390501) |
| Manufacturer | Roche Diagnostics GmbH, Alemania |
| Models | 2.2.0, E-08174, 171-173, WIN10, SOFTWARE2.2.0, 2021-321.LA, B61503355, 70401, 2021-321, 2.3.7, 71321, B-173656 and 16 more |
| Event type | Safety Notice |
| Date | Jul 8, 2021 |
At a glance
- No Recall
- Yes 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