13 results
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20ms
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Sources: EU EUDAMED, US FDA
ANALOG QUANTIFIER MODEL AQ-100
FDA 510(k)
FDA Class 2
·Neurology
ELEVATE™ Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169430679·SPACER 7771023 ELEVATE STD 23X10MM
NA
FDA UDI
KEY SURGICAL, INC.·10849771048753·K-Wires, Double trocar, .045-inch (1.1mm) diame...
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704292381·
mahe medical GmbH
FDA UDI
mahe medical gmbh·04050659483934·K-Wire w. double end trocarpoint _x000D_...
K-Wire w. double end trocarpoint 1.10mm/152mm, 6 pcs./unit
FDA UDI
mahe medical gmbh·EMAHKM710230·K-Wire w. double end trocarpoint
1.10mm...
SIMULATOR, 10 LEAD ECG
FDA 510(k)
FDA Class 2
·Cardiovascular
REACH RCS CIRCULAR STAPLER, MODEL RCS21C, RCS25C, RCS28C, RCS31C, RCS34C
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ELEVATE SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code MAX·September 25, 2024
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·October 3, 2012
ALLEGRETTO WAVE EYE-Q
FDA Adverse Event
Injury
·WAVELIGHT GMBH·Product code LZS·December 18, 2013
MYNX VASCULAR CLOSURE DEVICE
FDA Adverse Event
Injury
·ACCESSCLOSURE, INC.·Product code MGB·July 27, 2010
ELEVATE SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code MAX·May 15, 2021