International Medical Devices Database

Manufacturer Parent Company (2017)
Bio-Rad Laboratories Inc
Source
HA
1 Event
- Recall of ID-DiaCell I-II, ID-DiaCell ABO/I-II

One device in the database

ID-DiaCell I-II, ID-DiaCell ABO/I-II

Model / Serial
Product Description
Warning reactive id diacell - diamed

26 manufacturers with a similar name

Learn more about the data here

BIO-RAD y DIAMED GmbH || Imported by: BIOCIENTIFICA LTDA.

Manufacturer Parent Company (2017)
Bio-Rad Laboratories Inc
Source
NIDFSINVIMA

DiaMed GmbH

Manufacturer Parent Company (2017)
Bio-Rad Laboratories Inc.
Source
FSSH

Diamed GMBH

Manufacturer Parent Company (2017)
Bio-Rad Laboratories Inc
Source
AEMPSVFOI

Diamed GmbH

Manufacturer Parent Company (2017)
Bio-Rad Laboratories Inc
Source
AEMPSVFOI

DiaMed GmbH

Manufacturer Parent Company (2017)
Bio-Rad Laboratories Inc
Source
AEMPSVFOI

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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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