2,442 results · 33ms · 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.

Miracle-Ear

FDA UDI
Ws Audiology Usa, Inc.·04038953848840·Miracle-Ear ECHARGER 013-K ME NTS. Hearing aid...

TARGET DEVICE 300 X 160 MM

FDA Adverse Event
Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·August 8, 2011

GUIDE WIRE SLEEVE 10.5X268MM

FDA Adverse Event
Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·October 14, 2011

NEOWRAP

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE, LTD.·Product code KME·February 4, 2009

NEOWRAP

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE, LTD.·Product code KME·February 4, 2009

NEOWRAP

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE, LTD.·Product code KME·February 4, 2009

CAPRI BLADDER CONTROL PADS

FDA Adverse Event
Malfunction ·MEDLINE INDUSTRIES INC.·Product code KME·December 13, 2016

DISPOSABLE RECEIVING SHEET

FDA Adverse Event
GLOBAL HEALTHCARE·Product code KME·April 10, 2012

OASIS ELITE

FDA Adverse Event
Injury ·TRULIFE·Product code KME·October 6, 2003

MICROTEK

FDA Adverse Event
Malfunction ·MICROTEK MEDICAL B.V.·Product code KME·July 2, 2024

THERMOFLECT

FDA Adverse Event
Injury ·ENCOMPASS THERAPUTIC SUPPORT SYSTEMS·Product code KME·December 4, 2009

THERMOFLECT

FDA Adverse Event
Injury ·INDUSTRIA MANUFACTUREAS DE TAMAULIPAS, SA DE C.V.·Product code KME·December 22, 2009

MATTRESS SHEETS (DISPOSABLE), 46' X 84"

FDA Adverse Event
Injury ·GLOBAL HEALTHCARE·Product code KME·November 16, 2010

GLOBAL HEALTHCARE MATTRESS SHEET

FDA Adverse Event
GLOBAL HEALTHCARE·Product code KME·November 23, 2010

MAXISLIDE

FDA Adverse Event
Other ·ARJO, LTD.·Product code KME·December 13, 2000

CLEANOP INFECTION CONTROL SYSTEM

FDA Adverse Event
Malfunction ·ECOLAB/MICROTEK MEDICAL·Product code KME·August 5, 2020

CLEANOP INFECTION CONTROL SYSTEM

FDA Adverse Event
Malfunction ·ECOLAB/MICROTEK MEDICAL IN.·Product code KME·August 25, 2020

STAPH CHECK II PILLOW

FDA Adverse Event
Malfunction ·HERCULITE PRODUCTS, INC.·Product code KME·August 28, 1997

LIFT SHEET INCLUDED IN A CLEAN UP INFECTION CONTROL SYSTEM

FDA Adverse Event
MICROTEK MEDICAL, INC.·Product code KME·December 15, 2010

MICROTEK

FDA Adverse Event
Malfunction ·ECOLAB/MICROTEK MEDICAL INC.·Product code KME·April 18, 2022