Devices

Device Recall Acute Care CCRP CalPak

Model / Serial
Lot Numbers: 625229002
Product Classification
Immunology and Microbiology Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution - US (nationwide), Algeria, Armenia, Australia, Austria, Bangladesh, Bosnia Herzegovina, Canada, Croatia, Czech Republic, Denmark, Finland, France, Germany, Greece, India, Ireland, Italy, Japan, Libya, Malaysia, Poland, Portugal, Romania, Saudi Arabia, Slovenia, South Africa, Spain, Sweden, Switzerland, Taiwan, Turkey, U.A.E., and United Kingdom.
Product Description
Siemens Acute Care CCRP CalPak-in vitro diagnostic product intended to be used for calibration of the CCRP method on the Stratus CS analyzer || Catalog Number: CCCRP-C || SMN:10445067
Manufacturer
Siemens Healthcare Diagnostics Inc
1 Event
- Recall of Device Recall Acute Care CCRP CalPak

Manufacturer

Siemens Healthcare Diagnostics Inc

Manufacturer Address
Siemens Healthcare Diagnostics Inc, 2 Edgewater Dr, Norwood MA 02062-4637
Manufacturer Parent Company (2017)
Siemens Ag
Source
USFDA

One device with a similar name

Learn more about the data here

Device Recall Acute Care CCRP CalPak

Model / Serial
Lot Number: 425229002
Product Classification
Immunology and Microbiology Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution - US (nationwide), Algeria, Armenia, Australia, Austria, Bangladesh, Bosnia Herzegovina, Canada, Croatia, Czech Republic, Denmark, Finland, France, Germany, Greece, India, Ireland, Italy, Japan, Libya, Malaysia, Poland, Portugal, Romania, Saudi Arabia, Slovenia, South Africa, Spain, Sweden, Switzerland, Taiwan, Turkey, U.A.E., and United Kingdom.
Product Description
Siemens Acute Care" CCRP TestPak-in vitro diagnostic product intended to be used for calibration of the CCRP method on the Stratus¿ CS analyzer || Catalog Number: CCCRP || SMN:10445066
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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