26 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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