14 results
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32ms
·
Sources: EU EUDAMED, US FDA
PHOTOTHERAPY/PROCEDURE LAMP
FDA 510(k)
FDA Class 2
·General Hospital
CoRoent
FDA UDI
Nuvasive, Inc.·00887517809674·Interlock II, 10x17x14mm 25°
NA
FDA UDI
KEY SURGICAL, INC.·10849771048777·K-Wires, Double trocar, .062-inch (1.6mm) diame...
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704292404·
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·14026704912268·
K-Wire w. double end trocarpoint 1.60mm/152mm, 6 pcs./unit
FDA UDI
mahe medical gmbh·EMAHKM710250·K-Wire w. double end trocarpoint
1.60mm...
mahe medical GmbH
FDA UDI
mahe medical gmbh·04050659483958·K-Wire w. double end trocarpoint _x000D_...
ZOLL AEDPRO WITH SEE-THRU CPR, MODEL AEDPRO
FDA 510(k)
FDA Class 3
·Cardiovascular
BAG RESUSCITATOR
FDA 510(k)
FDA Class 2
·Anesthesiology
GORE® TAG® THORACIC ENDOPROSTHESIS
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code MIH·November 23, 2015
SPECTRA OPTIA
FDA Adverse Event
TERUMO BCT·Product code LKN·October 3, 2012
WAVELIGHT EX500 EXCIMER LASER
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
Azurion 7 M12; System Code: (1)722078, (2)722223, (3)722233;
FDA Enforcement
Class II
·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·April 8, 2026