21 results
·
31ms
·
Sources: EU EUDAMED, US FDA
ROYALE BRAND LATEX CONDOMS (SILICONE)-COLORED/ASSORTED COLORS
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
NA
FDA UDI
KEY SURGICAL, INC.·10849771049040·K-Wires, Single trocar, .045-inch (1.1mm) diame...
Key Surgical K-Wires and Steinmann Pins
FDA UDI
KEY SURGICAL, INC.·00849771012467·K-Wires, Single trocar, .045-inch (1.1mm) diame...
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·14026704912374·
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704292695·
K-Wire w. trocar/round end 1.14mm/102mm, 6 pcs./unit
FDA UDI
mahe medical gmbh·EMAHKM711320·K-Wire w. trocar/round end
1.14mm...
mahe medical GmbH
FDA UDI
mahe medical gmbh·04050659484238·K-Wire w. trocar/round end _x000D_...
G8 AUTOMATED HPLC ANALYZER, MODEL HLC-723 G8
FDA 510(k)
FDA Class 2
·Hematology
Carefusion NeutraClear Needle-free connector
FDA 510(k)
FDA Class 2
·General Hospital
INRATIO PT/INR TEST STRIP
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code GJS·April 29, 2014
PLUM 1.6 W/ DATAPORT
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·February 1, 2013
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·COCHLEAR LTD.·Product code MCM·January 26, 2011
LINER NEUTRAL 36 MM I.D. SIZE NN FOR USE WITH 62 MM O.D. SIZE NN SHELL
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·April 25, 2019
TOSOH HLC-723G8 ANALYZER
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code LCP·December 20, 2017
TOSOH HLC-723G8 ANALYZER
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code LCP·December 15, 2017
TOSOH HLC-723G8 ANALYZER
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code LCP·December 20, 2017
TOSOH HLC-723G8 ANALYZER
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code LCP·December 11, 2017
TOSOH HLC-723G8 ANALYZER G8
FDA Adverse Event
Injury
·TOSOH CORPORATION·Product code LCP·January 5, 2016
TOSOH HLC-723G8 ANALYZER G8
FDA Adverse Event
Injury
·TOSOH CORPORATION·Product code LCP·January 3, 2017
IMPLANTABLE NEUROSTIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LGW·November 28, 2023