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

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GMRS PRESS FIT STEMS WITH PUREFIX HA

FDA 510(k)
FDA Class 2 ·Orthopedic

Cook

FDA UDI
COOK INCORPORATED·00827002148901·Laser Ureteral Catheter

Cook

FDA UDI
COOK INCORPORATED·00827002188839·Laser Ureteral Catheter

Cook

FDA UDI
COOK INCORPORATED·00827002150201·Laser Ureteral Catheter

VANGUARD REPROCESSED COMPRESSION GARMENT

FDA 510(k)
FDA Class 2 ·Cardiovascular

NOVOFINE 31 DISPOSABLE NEEDLE

FDA 510(k)
FDA Class 2 ·General Hospital

Cook

FDA UDI
COOK INCORPORATED·00827002177970·Laser Ureteral Catheter

SMART MONITOR 2 PS

FDA Adverse Event
Malfunction ·PHILIPS RESPIRONICS -CHMV·Product code NPF·August 26, 2014

M-H HA/PC 11X160MM T1

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code LPH·December 16, 2015

M-H SOLID SHELL HA/PC DIA54MM LN24

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code LPH·March 1, 2016

MALLORY-HEAD SHORT FEMORAL STEM

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code MEH·July 28, 2017

IMMULITE 2000

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code CFP·January 23, 2012

IMMULITE 2000

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code CFP·February 2, 2012

MALLORY-HEAD ACETABULAR SHELL 54MM POUROUS + HAP COATED

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code MEH·August 11, 2016

EON MINI

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 22, 2013

TOTALCARE

FDA Adverse Event
Malfunction ·HILL-ROM INC.·Product code FNL·February 16, 2011

EMBRACE PUMP

FDA Adverse Event
Malfunction ·Product code LZH·March 26, 2008

MLRY-HD XR LAT POR FMRL 8MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·August 24, 2020

IMMULITE 2000 INSULIN

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS·Product code CFP·January 27, 2012

IMMULITE 2000 INSULIN

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS·Product code CFP·February 1, 2012