Devices

Device Recall CEA ELISA Kit

Model / Serial
Catalog number: BC-1011; RN-33968 04-2010 RN-34421 06-2010 RN-34473 06-2010 RN-34853 07-2010 RN-35157 08-2010 RN-35486 08-2010 RN-35815 09-2010 RN-36179 12-2010 RN-36221 12-2010 RN-36751 02-2011 RN-37124 02-2011 RN-37125 02-2011 RN-37892 05-2011 RN-37953 02-2011 RN-38320 07-2011 RN-38307 07-2011 RN-39144 08-2011 RN-39416 10-2011 RN-39417 10-2011 RN-40110 12-2011 RN-40464 12-2011 RN-40982 04-2012 RN-41177 04-2012.
Product Classification
Immunology and Microbiology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide distribution.
Product Description
CEA ELISA Kit. || BioCheck, Foster City, CA 9440. || Quantitative determination of AFP concentration in human serum.
Manufacturer
BioCheck Inc
1 Event
- Recall of Device Recall CEA 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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