International safety notice
• Módulo e801 del inmunoanalizador modular cobas 8000, modelo 08454345001 • Reactivo ProCell II M, modelo 06908799190, utilizado en los módulos cobas e801
Spain / AEMPS · ESP · Apr 3, 2019
Key facts
| Title | • Módulo e801 del inmunoanalizador modular cobas 8000, modelo 08454345001 • Reactivo ProCell II M, modelo 06908799190, utilizado en los módulos cobas e801 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | • Módulo e801 del inmunoanalizador modular cobas 8000, modelo 08454345001 • Reactivo ProCell II M, modelo 06908799190, utilizado en los módulos cobas e801 |
| Manufacturer | Hitachi High-Technologies Corporation (HHT), Japón. |
| Models | 345-000001, T30354, E-08174, 51075, 06908799190, 07682913001, 171-173, HSV-2, SBN-CPS-2018-025, SFLT-1, 744-XXXXXX, B61503355 and 15 more |
| Event type | Safety Notice |
| Date | Apr 3, 2019 |
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