21 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Carefusion NeutraClear Needle-free connector
FDA 510(k)
FDA Class 2
·General Hospital
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
POWDER FREE VINYL PATIENT EXAMINATION GLOVES, (BLUE, WHITE, PINK)
FDA 510(k)
FDA Class 1
·General Hospital
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·June 14, 2013
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code MDS·July 11, 2011
LAP BAND ADJUSTABLE GASTRIC BANDING SYSTEM
FDA Adverse Event
Injury
·BIOENTERICS CORP·Product code LTI·September 18, 2008
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
TOSOH HLC-723G8 ANALYZER G8
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code LCP·April 16, 2018
BD¿ SYRINGE WITH NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMF·March 15, 2018