Devices

Device Recall Desktop Pro Linear Medical Accelerator

Model / Serial
Model number MRT 9871/ MRT 10601 (This issue affects Desktop Pro 6.0 and 6.1 users with a 3rd party R & V System, with the exception of Sigma Micro Users)
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide distribution ---- including USA states of AZ, AL, CA, CO, FL, GA, IA, MI, NV, OH, OK, PA, WA, WV and Country of Canada .
Product Description
Desktop Pro¿ R6.0 & R6.1, Linear Medical Accelerator.
Manufacturer
Elekta, Inc.
1 Event
- Recall of Device Recall Desktop Pro Linear Medical Accelerator

Manufacturer

Elekta, Inc.

Manufacturer Address
Elekta, Inc., 4775 Peachtree Industrial Blvd., Building 300, Suite 300, Norcross GA 30092-3023
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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