Devices

Device Recall CA199 ELISA Kit

Model / Serial
Catalog number: BC-1017; RN-34237 05-2010 RN-33400 02-2010 RN-34586 05-2010 RN-34850 05-2010 RN-35131 08-2010 RN-35474 09-2010 RN-35854 09-2010 RN-36593 01-2011 RN-37142 03-2011 RN-37903 04-2011 RN-39461 09-2011 RN-40394 02-2012 RN-40916 04-2012.
Product Classification
Immunology and Microbiology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide distribution.
Product Description
CA19-9 ELISA Kit. || BioCheck, Foster City, CA 9440. || Quantitative determination of AFP concentration in human serum.
Manufacturer
BioCheck Inc
1 Event
- Recall of Device Recall CA199 ELISA Kit

Manufacturer

BioCheck Inc

Manufacturer Address
BioCheck Inc, 323 Vintage Park Dr, Foster City CA 94404-1186
Manufacturer Parent Company (2017)
Origene Technologies Inc
Source
USFDA

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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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