11 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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B-D ULTRA-VUE PROCEDURE NEEDLE W/ SPINAL TYPE PT.
FDA 510(k)
FDA Class 2
·Cardiovascular
SPIROSCOPE
FDA 510(k)
FDA Class 2
·Anesthesiology
FLEXIBLE CHOLEDOCHOSCOPE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
TANDEM T:SLIM INSULIN DELIVERY SYS
FDA Adverse Event
Malfunction
·TANDEM DIABETES·Product code LZG·June 5, 2014
HUDSON STERILE WATER AQUAPAK HUMIDIFIER 650 ML
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code CAF·November 5, 2010
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCO·Product code CBK·January 10, 2013
ARCOMXL 32MM RLC LNR MROM SZ23
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LZO·June 18, 2018
CER BIOLOXD OPTION HD 32MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LZO·June 18, 2018
FREEDOM CONSTR. LINER +5 SZ 23
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWZ·January 11, 2018
FREEDOM CONSTR HD 36MM T1 STD
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWZ·January 11, 2018
BIOMET StageOne Knee Femoral Cement Spacer Mold, 75 MM, Silicone, Sterile, Item 432175.
FDA Enforcement
Class II
·Terminated·Biomet, Inc.·April 15, 2020