Device product
Carl Zeiss INTRABEAM PRS 500, product #304534-0000-500. The firm name on the label is Carl Zeiss Meditec AG, Jena, Germany. The INTRABEAM System is indicated for radiation therapy treatments
Z-0001-2018
Product summary
- Event
- Event 78082
- Status
- Terminated
- Classification
- Class II
- Quantity
- 9 devices
- Official record key
device-enforcement:Z-0001-2018
Official wording
Reason: The device had an incorrect printed calibration value on the calibration certificate.
Code information: Intrabeam ser. #6402501246, Ion chamber ser. #SN001254; Intrabeam ser. #6402501241, Ion chamber ser. #SN001745; Intrabeam ser. #6402100932, Ion chamber ser. #SN001994; Intrabeam ser. #6402100958, Ion chamber ser. #SN002096; Intrabeam ser. #6402101042, Ion chamber ser. #SN002265; Intrabeam ser. #6402101029, Ion chamber ser. #SN002270; Intrabeam ser. #6402101034, Ion chamber ser. #SN002302; Intrabeam ser. #6402101105, Ion chamber ser. #SN002651; and Intrabeam ser. #6402101130, Ion chamber ser. #SN002684.
Distribution pattern: Nationwide Distribution including AZ, CA, CT, DC, FL, GA, OH, and PA.
Derived failure modes
-
Unknown
The device had an incorrect printed calibration value on the calibration certificate.