International Medical Devices Database

Manufacturer Parent Company (2017)
Compagnie Merieux Alliance
Source
NOM
1 Event
- Recall of VITEK® 2 Gram-Positive (GP) Identification (ID) Test Kit (code 21342) batches 2420240403 and 2120303403

One device in the database

VITEK® 2 Gram-Positive (GP) Identification (ID) Test Kit (code 21342) batches 2420240403 and 2120...

Model / Serial
Product Description
Recall of batches 2420240403 and 2120303403 of the in vitro diagnostic medical device VITEK® 2 Gram-Positive (GP) Identification (ID) Test Kit (code 21342)

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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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BIOMÉRIEUX INC, USA

One device in the database

VITEK® 2 Gram-Positive (GP) Identification (ID) Test Kit (code 21342) batches 2420240403 and 2120...