International Medical Devices Database

Manufacturer Parent Company (2017)
DiaSorin SpA
Source
AEMPSVFOI
1 Event
- Recall Or Safety Alert for LIAISON® Estradiol II Gen. Assay

One device in the database

LIAISON® Estradiol II Gen. Assay

Model / Serial

6 manufacturers with a similar name

Learn more about the data here

Diasorin Inc.

Manufacturer Address
Diasorin Inc., 1951 Northwestern Ave S, Stillwater MN 55082-7536
Manufacturer Parent Company (2017)
DiaSorin SpA
Source
USFDA

DiaSorin Inc. US

Manufacturer Parent Company (2017)
DiaSorin SpA
Source
BAM

DiaSorin Inc.

Manufacturer Parent Company (2017)
DiaSorin SpA
Source
SMPA

DIASORIN INC.

Manufacturer Address
STILLWATER
Manufacturer Parent Company (2017)
DiaSorin SpA
Source
HC

Diasorin Inc.

Manufacturer Address
Diasorin Inc., 1951 Northwestern Ave S, P.O Box 285, Stillwater MN 55082-7536
Source
USFDA

One more

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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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