Devices

Device Recall MARS Treatment Kit

Model / Serial
UDI: 37332414107728; Lot Numbers: 0000022597, 0000022648, 0000022663, 0000022671, 0000022721, 0000022767
Product Classification
Gastroenterology-Urology Devices
Device Class
2
Implanted device?
No
Distribution
US, Germany, Sweden, Italy, Belgium, Portugal, Spain, France, Russia, Poland, Turkey, China, Thailand, Taiwan, Hong Kong, Malaysia, Korea, and Mexico.
Product Description
MARS Treatment Kit, Use only with MARS(R) Monitor 1TC, GAMBRO, Product Code 800541
Manufacturer
Baxter Healthcare Corporation
1 Event
- Recall of Device Recall MARS Treatment Kit

Manufacturer

Baxter Healthcare Corporation

Manufacturer Address
Baxter Healthcare Corporation, 1 Baxter Pkwy, Deerfield IL 60015-4625
Manufacturer Parent Company (2017)
Baxter International
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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