51 results · 22ms · Sources: EU EUDAMED, US FDA

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STELLARIS PC VISION ENHANCEMENT SYSTEM

FDA 510(k)
FDA Class 2 ·Ophthalmic

AGXO

FDA UDI
Oticon A/S·05707131261816·H100, BTE 13 WL 85 SIL AGXO

GE PRECISION MPI

FDA 510(k)
FDA Class 2 ·Radiology

VOLCANO S5I INTRAVASCULAR ULTRACOUND IMAGING AND PRESSURE SYSTEM

FDA 510(k)
FDA Class 2 ·Radiology

DUO FLUID CART

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·December 21, 2017

ULTRA DUO HIGH FLUID CART NON-STERILE INSTRUCTIONS FOR USE

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·August 31, 2018

UNK MAMMARY IMPLANT

FDA Adverse Event
Injury ·ALLERGAN·Product code FWM·May 24, 2013

BRACHYVISION

FDA Adverse Event
Injury ·VARIAN MEDICAL SYSTEMS FINLAND OY·Product code MUJ·June 15, 2011

HYDRATOME RX SPHINCTEROTOME

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·August 22, 2008

ULTRAFLEX DUO HIGH FLUID CART - REFURBISHED

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·June 25, 2020

TRIATHLON P/A CR BEADED #5L

FDA Adverse Event
Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MBH·January 29, 2024

EVAC STATION

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·September 5, 2017

ULTRAFLEX DUO HIGH FLUID CART WITH SMOKE EVACUATOR

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·January 11, 2018

EVAC STATION

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·January 16, 2018

ULTRA DUO HIGH FLUID CART NON-STERILE INSTRUCTIONS FOR USE

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·June 7, 2018

ULTRAFLEX DUO HIGH FLUID CART WITH SMOKE EVACUATOR

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·August 3, 2017

ULTRA DUO HIGH FLUID CART NON-STERILE INSTRUCTIONS FOR USE

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·March 19, 2018

ULTRA DUO HIGH FLUID CART

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·December 27, 2017

ULTRA DUO HIGH FLUID CART NON-STERILE INSTRUCTIONS FOR USE

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·October 9, 2018

TRIATHION

FDA Adverse Event
Injury ·HOWMEDICA OSTEONICS CORP.·Product code JWH·December 14, 2023