Devices

8578: Suturless Pump Connector Revision Kit

Model / Serial
All lots numbers included
Product Classification
General Hospital and Personal Use Devices
Device Class
3
Implanted device?
Yes
Distribution
International Distribution --- country of Belgium.
Product Description
Medtronic 8578 Sutureless Pump Connector Revision Kit || Medtronic Inc., Minneapolis, MN 55432 || A part of the SynchroMed II Infusion system, which is designed to restore and provide intrathecal administration of drug therapy.
Manufacturer
Medtronic Neuromodulation
1 Event
- Recall of 8578: Suturless Pump Connector Revision Kit

Manufacturer

Medtronic Neuromodulation

Manufacturer Address
Medtronic Neuromodulation, 800 53rd Ave NE, PO Box 1250, Minneapolis MN 55440-1250
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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