Devices

Device Recall Siemens ADVIA Centaur iPTH ReadyPack Assay

Model / Serial
Reagent Lot Numbers: 056301 and 56302 Kit Lot Number/Exp. Date: REF 10492369- 500 Tests 61639301 09 Nov 2011 REF 1 0493615 - 500 Tests 63607301 09 Nov 2011 68004301 09 Nov 2011 70229301 09 Nov 2011 74126301 09Nov2011 REF 10493616-500 Tests 62645302 09 Nov 2011 66612302 09 Nov 2011 74129302 09 Nov 2011
Product Classification
Clinical Chemistry and Clinical Toxicology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution.
Product Description
ADVIA Centaur¿ iPTH ReadyPack Assay 500 Tests; REF 10492369, 10493615, 1049361. || For in vitro diagnostic use in the quantitative determination of intact parathyroid hormone (iPTH).
Manufacturer
Siemens Healthcare Diagnostics, Inc
1 Event
- Recall of Device Recall Siemens ADVIA Centaur iPTH ReadyPack Assay

Manufacturer

Siemens Healthcare Diagnostics, Inc

Manufacturer Address
Siemens Healthcare Diagnostics, Inc, 333 Coney St, East Walpole MA 02032-1516
Manufacturer Parent Company (2017)
Siemens Ag
Source
USFDA

One device with a similar name

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Device Recall Siemens ADVIA Centaur iPTH ReadyPack Assay

Model / Serial
Reagent Lot Number: 056301 and 56302 Kit Lot Number/Exp. Date: 61655301 09 Nov 2011 61950302 09 Nov 2011
Product Classification
Clinical Chemistry and Clinical Toxicology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution.
Product Description
ADVIA Centaur¿ iPTH ReadyPack Assay 100 Tests; REF 10492368. || For in vitro diagnostic use in the quantitative determination of intact parathyroid hormone (iPTH).
Manufacturer
Siemens Healthcare Diagnostics, Inc

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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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