18 results · 27ms · Sources: EU EUDAMED, US FDA

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Omnitech HF Resection Electrodes, Omnitech HF Vaporization Electrode

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

INTERFACE ACETABULAR SYSTEM, ACETABULAR INSERT +4 OFFSET

FDA 510(k)
FDA Class 2 ·Orthopedic

PROVEN REVISION MODULAR TIBIAL TRAY

FDA 510(k)
FDA Class 2 ·Orthopedic

HISTOACRYL FLEXIBLE PACK 5

FDA Adverse Event
Injury ·B.BRAUN SURGICAL SA·Product code MPN·July 23, 2019

KRD DEVICE, EMBOLIZATION, VASCULAR

FDA Adverse Event
Malfunction ·COOK INC·Product code KRD·September 19, 2019

ALLEGRETTO WAVE EYE-Q

FDA Adverse Event
Injury ·WAVELIGHT GMBH·Product code LZS·October 6, 2014

DRUG ELUTING PERMANENT LEFT VENTRICULAR (LV) PACEMAKER ELECTRODE

FDA Adverse Event
Injury ·RICE CREEK MFG·Product code OJX·June 7, 2013

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 7, 2011

VITEK® 2 AST-ST01 TEST KIT

FDA Adverse Event
Malfunction ·BIOMERIEUX, INC·Product code LON·October 24, 2017

RETRACTA DETACHABLE EMBOLIZATION COIL

FDA Adverse Event
Injury ·COOK INC·Product code KRD·June 20, 2019

RETRACTA DETACHABLE EMBOLIZATION COIL

FDA Adverse Event
Malfunction ·COOK INC·Product code KRD·September 17, 2018

RETRACTA DETACHABLE EMBOLIZATION COIL

FDA Adverse Event
Malfunction ·COOK INC·Product code KRD·September 17, 2018

RETRACTA DETACHABLE EMBOLIZATION COIL

FDA Adverse Event
Malfunction ·COOK INC·Product code KRD·January 2, 2020

RETRACTA DETACHABLE EMBOLIZATION COIL

FDA Adverse Event
Malfunction ·COOK INC·Product code KRD·January 2, 2020

RETRACTA DETACHABLE EMBOLIZATION COIL

FDA Adverse Event
Malfunction ·COOK INC·Product code KRD·March 11, 2020

RETRACTA DETACHABLE EMBOLIZATION COIL

FDA Adverse Event
Malfunction ·COOK INC·Product code KRD·July 31, 2019

RETRACTA DETACHABLE EMBOLIZATION COIL

FDA Adverse Event
Injury ·COOK INC·Product code KRD·February 25, 2019

RETRACTA DETACHABLE EMBOLIZATION COIL

FDA Adverse Event
Malfunction ·COOK INC·Product code KRD·February 3, 2020