Devices

Device Recall CKMB ELISA kit

Model / Serial
Catalog number: BC-1121: RN-33897 04-2010 RN-34288 04-2010 RN-35945 11-2010 RN-36594 01-2011 RN-38211 07-2011 RN-39307 07-2011 RN-39618 07-2011 RN-40219 01-2012 RN-41069 01-2012.
Product Classification
Clinical Chemistry and Clinical Toxicology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide distribution.
Product Description
CK-MB ELISA kit ; || BioCheck, Foster City, CA 9440. || Quantitative determination of AFP concentration in human serum.
Manufacturer
BioCheck Inc
1 Event
- Recall of Device Recall CKMB 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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