International Medical Devices Database

Manufacturer Address
Sakura Finetek USA Inc, 1750 W 214th St, Torrance CA 90501-2857
Manufacturer Parent Company (2017)
Sakura Global Holding Co. Ltd.
Source
USFDA
1 Event
- Recall of TissueTek PARAFORM PROC/EMB/MEDIUM

One device in the database

TissueTek PARAFORM PROC/EMB/MEDIUM

Model / Serial
Product Code: 7052. Lot Number: 263922.
Product Classification
Hematology and Pathology Devices
Device Class
1
Implanted device?
No
Distribution
Nationwide Distribution.
Product Description
Tissue-Tek PARAFORM PROC/EMB/MEDIUM, FORMULA 3 - 8x1Kg. || for diagnostic chemistry use. || Sakura Finetek USA, Inc.

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Disclaimer

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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Sakura Finetek USA Inc

One device in the database

TissueTek PARAFORM PROC/EMB/MEDIUM