11 results
·
32ms
·
Sources: EU EUDAMED, US FDA
BCD PLUS BLOOD CARDIOPLEGIA SYS(HEREAF REFER DEV)
FDA 510(k)
FDA Class 2
·Cardiovascular
NAR Kit
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209111251·KIT, CUSTOM SAMPLES KIT
DENTAPLAST HOT, MODEL 16-XXX
FDA 510(k)
FDA Class 2
·Dental
LCD Monitor (CL1902A, CL2103F)
FDA 510(k)
FDA Class 2
·Radiology
OT PING ENHANCED METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2014
LYNX SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·November 30, 2012
TANDEM T:SLIM INSULIN DELIVERY SYSTEM
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE INC.·Product code LZG·June 17, 2015
OSS POLY TIBIAL BUSHING
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·February 13, 2020
OSS POLY LOCK PIN
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·February 13, 2020
OSS 7CM SEG ELLIPT FEMORAL RT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·November 18, 2019
OSS TIBIAL POLY BEARING 12MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·November 18, 2019