International Medical Devices Database

Manufacturer Address
Separation Technology, Inc., 582 Monroe Rd Ste 1424, Sanford FL 32771-8821
Source
USFDA
1 Event
- Recall of Device Recall SLIDERPREP PLUS SLIDE PREPARATION CENTRIFUGE

One device in the database

Device Recall SLIDERPREP PLUS SLIDE PREPARATION CENTRIFUGE

Model / Serial
Serial numbers: 0110, 0111, 0112, 0210, 0211, 0212, 0310, 0311, 0312, 0410, 0411, 0412, 0511, 0512, 0611, 0710, 0711, 0811, 0812, 0910, 0911, 0912, 1011, 1012, 1112, 1210, 1212.
Product Classification
Hematology and Pathology Devices
Device Class
1
Implanted device?
No
Distribution
Worldwide Distribution-USA (nationwide) including the states of PA, NC, IL, KS, and FL, and the countries Canada and Turkey.
Product Description
SLIDERPREP PLUS SLIDE PREPARATION CENTRIFUGE. || Produce a monolayer of cells onto a glass slide from any fluid suspension.

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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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Separation Technology, Inc.

One device in the database

Device Recall SLIDERPREP PLUS SLIDE PREPARATION CENTRIFUGE