43 results · 23ms · Sources: EU EUDAMED, US FDA

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DIGITAL FLAT PLANEL X-RAY DETECTOR / 1717SCC

FDA 510(k)
FDA Class 2 ·Radiology

SPEACELABS MULTIGAS MODULE

FDA 510(k)
FDA Class 2 ·Anesthesiology

MOLDEX-METRIC HEALTH CARE N95 PARTICULATE RESPIRATOR AND SURGICAL MASK, MODEL 1712

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·March 30, 2026

DAILY ACTIVITY ASSIST DEVICES

FDA Adverse Event
Malfunction ·INVAMEX·Product code INB·October 31, 2011

DAILY ACTIVITY ASSIST DEVICES

FDA Adverse Event
POPULAR PLASTICS·Product code IKX·October 31, 2011

DAILY ACTIVITY ASSIST DEVICES

FDA Adverse Event
Malfunction ·INVAMEX·Product code INB·November 18, 2011

DAILY ACTIVITY ASSIST DEVICES

FDA Adverse Event
UNKNOWN·Product code IKX·June 8, 2012

DAILY ACTIVITY ASSIST DEVICES

FDA Adverse Event
UNKNOWN·Product code IKX·July 5, 2012

ACCESS

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - AIBONITO·Product code FPA·May 21, 2013

FATHOM GUIDEWIRE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - SALT LAKE CITY·Product code DQX·June 13, 2011

LINOX SD 65/16

FDA Adverse Event
Malfunction ·BIOTRONIK, GMBH AND CO.·Product code LWS·August 15, 2008

GLIDESHEATH SLENDER NITINOL (CONVENIENCE KIT)

FDA Adverse Event
Malfunction ·TERUMO MEDICAL CORPORATION·Product code DYB·February 21, 2018

DAILY ACTIVITY ASSIST DEVICES

FDA Adverse Event
POPULAR PLASTICS·Product code IKX·July 2, 2012

DAILY ACTIVITY ASSIST DEVICES

FDA Adverse Event
UNKNOWN·Product code IKX·June 7, 2012

DAILY ACTIVITY ASSIST DEVICES

FDA Adverse Event
UNKNOWN·Product code IKX·July 6, 2012

UNKNOWN OSS ORTHOPAEDIC SALVAGE SYSTEM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·October 23, 2017

UNKNOWN OSS ORTHOPAEDIC SALVAGE SYSTEM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·October 23, 2017

UNKNOWN OSS ORTHOPAEDIC SALVAGE SYSTEM

FDA Adverse Event
Death ·ZIMMER BIOMET, INC.·Product code JDI·October 23, 2017

DAILY ACTIVITY ASSIST DEVICES

FDA Adverse Event
UNKNOWN·Product code INN·April 4, 2012