50 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VBMAX
FDA 510(k)
FDA Class 2
·Anesthesiology
PowerPICC
FDA UDI
Bard Access Systems, Inc.·00801741129599·Catheter Placement Kit
TruForm
FDA UDI
Rmo, Inc.·00885797099594·MAN 1ST MOLAR LEFT 87 BANDS
RadialSeal™ Introducer Kit, Poly Wire
FDA UDI
Greatbatch Ltd·00821329400810·
RadialSeal™ Introducer Kit, Poly Wire
FDA UDI
Greatbatch Ltd·00821329000461·
RadialSeal™ Introducer Kit, Poly Wire
FDA UDI
Greatbatch Ltd·00821329000485·
RadialSeal™ Introducer Kit, Poly Wire
FDA UDI
Greatbatch Ltd·00821329400803·
RadialSeal™ Introducer Kit, Poly Wire
FDA UDI
Greatbatch Ltd·00821329400841·
RadialSeal™ Introducer Kit, Poly Wire
FDA UDI
Greatbatch Ltd·00821329400827·
RadialSeal™ Introducer Kit, Poly Wire
FDA UDI
Greatbatch Ltd·00821329400797·
RadialSeal™ Introducer Kit, Poly Wire
FDA UDI
Greatbatch Ltd·00821329400834·
RadialSeal™ Introducer Kit, Poly Wire
FDA UDI
Greatbatch Ltd·00821329000478·
FOAM CALCIUM ALGINATE TOPICAL WOUND DRESSING WITH COLLAGEN
FDA 510(k)
FDA Unclassified
·Unknown
ELIACHAR LARYNGEAL FOAM STENT, MODEL ELL-1
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
Alteon
FDA UDI
Exactech, Inc.·10885862555663·ALT CUP TRL G6 SIZE 54
KINETRA
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·February 17, 2014
ACTIVA
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MRU·September 23, 2015
SCREW LOCKING
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code HWC·March 14, 2012
SCREW
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code HWC·March 14, 2012
SCREW
FDA Adverse Event
Injury
·SYNTHES OBERDORF·Product code HWC·March 14, 2012