International Medical Devices Database

Manufacturer Parent Company (2017)
Werfenlife Sa.
Source
AEMPSVFOI
2 Events
- Recall Or Safety Alert for R ex-tem® reagent, reference 000503-05, lot 21734044
- Recall Or Safety Alert for ROTEM® sigma complete + hep cartridge, reference 555502.

2 devices in the database

R ex-tem® reagent, reference 000503-05, lot 21734044

Model / Serial

ROTEM® sigma complete + hep cartridge, reference 555502.

Model / Serial

12 manufacturers with a similar name

Learn more about the data here

Tem Innovations GmbH

Manufacturer Parent Company (2017)
Werfenlife Sa.
Source
FSSH

Tem Innovations Gmbh

Manufacturer Parent Company (2017)
Werfenlife Sa.
Source
LAANSM

TEM Innovations GmbH

Manufacturer Parent Company (2017)
Werfenlife Sa.
Source
BAM

Tem Innovations GmbH

Manufacturer Parent Company (2017)
Werfenlife Sa.
Source
BAM

Tem Innovations GmbH

Manufacturer Parent Company (2017)
Werfenlife Sa.
Source
AMPMDRS

About this database

Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

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