17 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Pivot System Sterilization case
FDA 510(k)
FDA Class 2
·General Hospital
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16741818450·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1674181845060·
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X1818450·18mm H x 18mm W x 45mm L x 0 degrees XLIF
SSW CARBIDE GREAT WHITE ULTRA
FDA UDI
Ss White Burs, Inc.·D6901818452·GREAT WHITE ULTRA CARBIDE GW856-020S - PACK 5
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X18184580·18mm H x 18mm W x 45mm L x 8 degrees XLIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X181845120·18mm H x 18mm W x 45mm L x 12 degrees XLIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587L181845120·18mm H x 18mm W x 45mm L XLIF Trial 12 degree L...
311NNM NARROWAND UV PHTOTHERAPY LIGHT LAMP
FDA Adverse Event
Injury
·XUZHOU KERNEL MEDICAL INSTRUMENT EQUIPMENT CO LTD.·Product code FTC·December 22, 2022
THE ESPINER SAC OR E SAC
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
IVENT101
FDA 510(k)
FDA Class 2
·Anesthesiology
MEDFUSION MODEL 4000 SYRINGE INFUSION PUMP
FDA Adverse Event
Malfunction
·ST PAUL·Product code FRN·January 13, 2023
VERIFLEX (TM)
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - GALWAY·Product code MAF·July 28, 2011
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·June 21, 2013
GE OEC 9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 19, 2008
EPIQ 7C ULTRASOUND CHINA LOCAL
FDA Adverse Event
Malfunction
·PHILIPS ULTRASOUND (SHANGHAI) CO., LTD·Product code IYN·June 2, 2023
Philips Zenition 70, Model Number: 718133
FDA Enforcement
Class II
·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·November 20, 2024