56 results · 20ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

RADIFOCUS GUIDEWIRE M

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·July 1, 2020

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 8, 2021

TERUMO RADIFOCUS GUIDE WIRE

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·May 12, 2025

A.L.P.S. CORTICAL LOCKING SCREW 3.5 MM X 34 MM

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code HRS·June 25, 2025

A.L.P.S PROXIMAL HUMERUS PLATING SYSTEM 3.2MM LOCKING PEG 40MM

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code HRS·June 25, 2025

A.L.P.S PROXIMAL HUMERUS PLATING SYSTEM 3.2MM LOCKING PEG 50 MM

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code HRS·June 25, 2025

A.L.P.S. CORTICAL LOCKING SCREW 3.5 MM X 28 MM

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code HRS·June 25, 2025

A.L.P.S. CORTICAL LOCKING SCREW 3.5 MM X 26 MM

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code HRS·June 25, 2025

A.L.P.S PROXIMAL HUMERUS PLATING SYSTEM 3.2MM LOCKING PEG 50 MM

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code HRS·June 25, 2025

A.L.P.S PROXIMAL HUMERUS PLATING SYSTEM 3.2MM LOCKING PEG 58 MM

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code HRS·June 25, 2025

A.L.P.S. CORTICAL LOCKING SCREW 3.5 MM X 44 MM

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code HRS·June 25, 2025

A.L.P.S. CORTICAL LOCKING SCREW 3.5 MM X 28 MM

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code HRS·June 25, 2025

A.L.P.S. CORTICAL LOCKING SCREW 3.5 MM X 46 MM

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code HRS·June 25, 2025

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·April 11, 2022

RADIFOCUS GUIDEWIRE M

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·March 15, 2023

RADIFOCUS GUIDEWIRE M

FDA Adverse Event
Malfunction ·TERUMO MEDICAL CORPORATION·Product code DQX·August 25, 2023

RADIFOCUS GUIDEWIRE M

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