Devices

Device Recall CA125 ELISA Kit

Model / Serial
Catalog number: BC-1013; RN-34041 04-2010 RN-34413 06-2010 RN-34847 06-2012 RN-35053 08-2010 RN-35341 08-2010 RN-35494 09-2010 RN-36176 12-2010 RN-36220 12-2010 RN-36733 02-2011 RN-37061 03-2011 RN-37755 05-2011 RN-38062 06-2011 RN-38866 08-2011 RN-39311 09-2011 RN-39691 11-2011 RN-39946 11-2011 RN-40220 01-2012 RN-40467 02-2012 RN-41008 04-2012 RN-41424 04-2012.
Product Classification
Immunology and Microbiology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide distribution.
Product Description
CA125 ELISA Kit. || BioCheck, Foster City, CA 9440. || Quantitative determination of AFP concentration in human serum.
Manufacturer
BioCheck Inc
1 Event
- Recall of Device Recall CA125 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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