International safety notice
Cobas® pure integrated solutions (cobas pure e 402), referencia 09031553001; Cobas® pro integrated solutions (cobas e 801), referencia 08454345001; Cobas® 8000 modular analyser series (cobas e 801), referencia 07682913001
Spain / AEMPS · ESP · Jul 20, 2022
Key facts
| Title | Cobas® pure integrated solutions (cobas pure e 402), referencia 09031553001; Cobas® pro integrated solutions (cobas e 801), referencia 08454345001; Cobas® 8000 modular analyser series (cobas e 801), referencia 07682913001 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Cobas® pure integrated solutions (cobas pure e 402), referencia 09031553001; Cobas® pro integrated solutions (cobas e 801), referencia 08454345001; Cobas® 8000 modular analyser series (cobas e 801), referencia 07682913001 |
| Manufacturer | Hitachi High Technologies Corporation (HHT), Japón |
| Models | 01-01, 08454345001, 28022, 07682913001, SBN-RDS-CORELAB-2022-004, 06-09, FSN-RDS-CORELAB-2022-004, T30354, 06-08, 81828, 02-02, 91.822.52.89 and 16 more |
| Event type | Safety Notice |
| Date | Jul 20, 2022 |
At a glance
- No Recall
- Yes Field safety notice
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