Devices

Device Recall Philips Bucky Diagnost

Model / Serial
Serial Numbers: 335292 351085 351326 348891 348895 353313 358016 359426 370503 354382 354749 369640 380748 356820 362256 357699 362257 357255 358489 380361 363543 362719 363669 363544 363305 363538 365150 364211 379698 380749 375725 375727 375729 377144 381880 381881 380798/SN07000617 381877 383767/SN07000639 392883/SN08000099 394519/SN08000135 421035/SN09000031 396577/SN08000190 402575/SN08000382 397513/SN08000185 407681/SN08000345 411751/SN08000438 410786/SN08000454 417251/SN08000547 427833/SN09000208 415998/SN08000511 416000/SN08000508 421979/SN09000098 422100/SN09000216 442036/SN09000336 448226/SN09000416 455130/SN10000286 462191/SN10000266 468071/SN10000398 467831/SN10000326 471707/SN11000023 477922/SN11000076 481951/SN11000205 489697/SN11000261
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution - US Nationwide and the country of Canada.
Product Description
Philips BuckyDiagnost Radiographic, a Diagnostic X-ray system. || Catalog Numbers: || 704031, 704032, 704035, 704060, 704062 || This system is used for making x-ray exposures for diagnostics.
Manufacturer
Philips Healthcare Inc.
1 Event
- Recall of Device Recall Philips Bucky Diagnost

Manufacturer

Philips Healthcare Inc.

Manufacturer Address
Philips Healthcare Inc., 3000 Minuteman Road, Andover MA 01810
Manufacturer Parent Company (2017)
Philips
Source
USFDA

One device with a similar name

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Device Recall Philips Bucky Diagnost FS

Model / Serial
Site numbers: 504495, 105355, 104447. The firm uses site numbers instead of serial numbers.
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
The firm distributed to three medical facilities in Florida, New York and California.
Product Description
Bucky Diagnost FS Part number 9890-010-83651
Manufacturer
Philips Medical Systems Sales & Service Region No. America

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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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