18 results · 28ms · Sources: EU EUDAMED, US FDA

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OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 22, 2013

RADIFOCUS GUIDEWIRE M

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·May 21, 2021

RADIFOCUS GUIDEWIRE M

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·April 12, 2021

RADIFOCUS GUIDEWIRE M

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·May 20, 2021

RADIFOCUS GUIDEWIRE M

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·November 6, 2018

RADIFOCUS GUIDEWIRE M

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·December 22, 2021

RADIFOCUS GUIDEWIRE M

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·May 15, 2019

RADIFOCUS GUIDEWIRE

FDA Adverse Event
Malfunction ·TERUMO MEDICAL CORPORATION·Product code DQX·March 26, 2024

RADIFOCUS GUIDEWIRE

FDA Adverse Event
Malfunction ·TERUMO MEDICAL CORPORATION·Product code DQX·February 8, 2024

RADIFOCUS GUIDEWIRE

FDA Adverse Event
Malfunction ·TERUMO MEDICAL CORPORATION·Product code DQX·March 12, 2024

RADIFOCUS GUIDEWIRE

FDA Adverse Event
Malfunction ·TERUMO MEDICAL CORPORATION·Product code DQX·March 12, 2024

RADIFOCUS GUIDEWIRE M

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·February 28, 2019

RADIFOCUS GUIDEWIRE M

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·February 22, 2019

RADIFOCUS GUIDEWIRE OR GLIDEWIRE OR GLIDEWIRE M

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·February 28, 2018

RADIFOCUS GUIDEWIRE

FDA Adverse Event
Malfunction ·TERUMO MEDICAL CORPORATION·Product code DQX·December 28, 2023

RADIFOCUS GLIDEWIRE

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·March 25, 2026

RADIFOCUS GLIDEWIRE

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·January 7, 2026

RADIFOCUS GUIDEWIRE M

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·July 8, 2019