19 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Fujifilm Diathermic Slitter (FlushKnife), Diathermic Slitter (ClutchCutter)
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Sonic
FDA UDI
Sonic Innovations, Inc.·05711583025148·CL100 MN, PS TT BE CELEBRATE 100
ProLift Trial
FDA UDI
Life Spine, Inc.·00190837088101·
HNM MEDICAL
FDA UDI
HNM STAINLESS, LLC.·00842962102022·ETHOS PRO SMALL JOINT ANCHOR, TITANIUM, 3.3mm x...
SYMBIOS DISPOSABLE INFUSION PUMP KIT
FDA 510(k)
FDA Class 2
·General Hospital
MD VISION SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
HNM MEDICAL
FDA UDI
HNM STAINLESS, LLC.·00842962104231·ETHOS PRO SMALL JOINT ANCHOR, TITANIUM, 3.3mm x...
RADIFOCUS GLIDEWIRE M
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DQX·January 22, 2018
PASSEO-18 5/200/90
FDA Adverse Event
Malfunction
·BIOTRONIK AG, BUELACH, SWITZERLAND·Product code LIT·September 28, 2021
PASSEO-18 6/200/90
FDA Adverse Event
Malfunction
·BIOTRONIK AG, BUELACH, SWITZERLAND·Product code LIT·September 28, 2021
PASSEO-18 2.5/170/130
FDA Adverse Event
Malfunction
·BIOTRONIK AG, BUELACH, SWITZERLAND·Product code LIT·January 20, 2021
ENDOTAK ENDURANCE
FDA Adverse Event
Malfunction
·CPI - DEL CARIBE·Product code NVY·July 6, 2011
CAPSUREFIX NOVUS
FDA Adverse Event
Death
·MPRI·Product code DTB·June 7, 2013
ORTHO SUMMIT SAMPLE HANDLING
FDA Adverse Event
Malfunction
·HAMILTON BONADUZ AG·Product code JTC·June 30, 2008
AXIUM
FDA Adverse Event
Malfunction
·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·October 10, 2019
AXIUM
FDA Adverse Event
Malfunction
·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·October 10, 2019
AXIUM
FDA Adverse Event
Malfunction
·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·October 10, 2019
AXIUM
FDA Adverse Event
Malfunction
·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·October 11, 2019
SL & SLi Series (Mod 15/18/20/25) Linear Accelerator Used for radiation therapy treatments of malignant neoplastics diseases.
FDA Enforcement
Class II
·Terminated·Elekta, Inc.·March 26, 2014