30 results · 26ms · Sources: EU EUDAMED, US FDA

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MICHELANGELO BUNION SYSTEM - MABS, MODEL: MA6000

FDA 510(k)
FDA Class 2 ·Orthopedic

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450584927·

OMNIDOS

FDA 510(k)
FDA Class 2 ·Radiology

CRIT-LINE MONITOR III (CLM III)

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

VASOVIEW 6 ACCESSORY PACK

FDA Adverse Event
Malfunction ·MAQUET CV·Product code GCJ·January 10, 2019

VASOVIEW 6 ACCESSORY PACK

FDA Adverse Event
Malfunction ·MAQUET CV·Product code GCJ·January 10, 2019

VASOVIEW 6 ACCESSORY PACK

FDA Adverse Event
Malfunction ·MAQUET CV·Product code GCJ·January 10, 2019

V SERIES MONITOR

FDA Adverse Event
Malfunction ·MINDRAY DS USA, INC.·Product code MHX·April 30, 2013

OVATIO

FDA Adverse Event
Injury ·SORIN CRM S.A.S.·Product code MRM·May 17, 2011

EBI OSTEOGEN IMPLANTABLE GROWTH STIMULATOR

FDA Adverse Event
Malfunction ·EBI, L.P.·Product code LOE·August 5, 2008

UNIVERSA SILICONE FOLEY CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZL·September 25, 2018

UNIVERSA SILICONE FOLEY CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZL·September 26, 2018

UPJ OCCLUSION BALLOON CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZN·April 7, 2017

UNIVERSA SILICONE FOLEY CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZL·July 8, 2019

UNIVERSA SILICONE FOLEY CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZL·November 14, 2017

UNIVERSA SILICONE FOLEY CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZL·November 19, 2018

UNIVERSA SILICONE FOLEY CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZL·July 19, 2018

UNIVERSA SILICONE FOLEY CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZL·August 1, 2018

UNIVERSA SILICONE FOLEY CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZL·August 22, 2018

UNIVERSA SILICONE FOLEY CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZL·February 21, 2018