Devices

Device Recall Ronci

Model / Serial
S/N''S: R00043, R001080, R001092, R001198, R0001341, R001370, R001374, R001366, R001337, R001497, R001478, R001493, R001501, R001529, R001812, R001816, R002023.
Product Classification
General Hospital and Personal Use Devices
Device Class
1
Implanted device?
No
Distribution
Nationwide. CA, FL, GA, IA MI, MT, NH, OH, NJ, NY, SC, UT, TX, VA
Product Description
Ronci Surgical Universal Imaging Extension used with the Ronci Pain Management Table System || Catalog Number: R-934-25A
Manufacturer
The OR Group
1 Event
- Recall of Device Recall Ronci

Manufacturer

The OR Group

Manufacturer Address
The OR Group, 531 Main St, Acton MA 01720-3934
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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