Devices

Device Recall Manual Method 1: 480 Test Kit (PreCoat)

Model / Serial
100903ru, 100924rr, 101022sc, 110114sh, 110225ru
Product Classification
Hematology and Pathology Devices
Device Class
3
Implanted device?
No
Distribution
Worldwide Distribution.
Product Description
Manual Method 1: 480 Test Kit (PreCoat), Catalog/Model # 490529
Manufacturer
Tripath Imaging, Inc.
1 Event
- Recall of Device Recall Manual Method 1: 480 Test Kit (PreCoat)

Manufacturer

Tripath Imaging, Inc.

Manufacturer Address
Tripath Imaging, Inc., 780 Plantation Dr, Burlington NC 27215-6723
Manufacturer Parent Company (2017)
Becton, Dickinson and Company
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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