11 results
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27ms
·
Sources: EU EUDAMED, US FDA
LITHIUM INTERNAL STANDARD 1 MEQ/L #60085
FDA 510(k)
FDA Class 2
·Clinical Chemistry
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704292916·
Key Surgical K-Wires and Steinmann Pins
FDA UDI
KEY SURGICAL, INC.·00849771012672·K-Wires, Single trocar, .062-inch (1.6mm) diame...
NA
FDA UDI
KEY SURGICAL, INC.·10849771049286·K-Wires, Single trocar, .062-inch (1.6mm) diame...
mahe medical GmbH
FDA UDI
mahe medical gmbh·04050659484467·K-Wire w. trocar/round end _x000D_...
K-Wire w. trocar/round end 1.57mm/152mm, 6 pcs./unit
FDA UDI
mahe medical gmbh·EMAHKM711850·K-Wire w. trocar/round end
1.57mm...
MODIFICATION TO: AMBU NEUROLINE, DISPOSABLE MONOPOLAR NEEDLE ELECTRODE
FDA 510(k)
FDA Class 2
·Neurology
IR Type Implant System
FDA 510(k)
FDA Class 2
·Dental
ARTICULEZE M HEAD 36MM +5
FDA Adverse Event
Malfunction
·DEPUY ORTHOPAEDICS INC US·Product code JDI·June 13, 2014
ENDOTAK RELIANCE
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVY·October 15, 2010
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 12, 2012