24 results
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30ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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POURCHEZ XPRESSO TWIN LIMEN CHRONIC HEMODIALYSIS CATHETER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
TAG
FDA UDI
Smith & Nephew, Inc.·03596010024749·TAG ABS ROD
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613019808·Dressing Forceps, Narrow,Curved, Serrated Jaws,...
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07310K0131100·Rod Inserter, Fixed, 90 Degree, MIS
FRYE & CO
FDA UDI
FGX INTERNATIONAL INC.·00193033483114·
Kalitec Special
FDA UDI
Kalitec Direct LLC·B073DRK0131100·Assembly, Rod Inserter, Fixed UNID
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0131100·Rocker, One Piece
Comfo-Tex™
FDA UDI
TETRA MEDICAL SUPPLY CORP.·00614138101630·COMFO-TEX ELASTIC BANDAGE LATEX FREE, 6INX5YD
E-Z EM PERCUPUMP 2001 CT INJECTOR
FDA 510(k)
FDA Class 2
·Radiology
WILLI GELLER CREAPEARL
FDA 510(k)
FDA Class 2
·Dental
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07310K0131300·Rod Inserter, Articulating, MIS
NA
FDA UDI
STRYKER CORPORATION·04546540346018·6.0mm XX-Coarse Diamond Round
NA
FDA UDI
STRYKER CORPORATION·04546540373113·6.0mm XX-Coarse Diamond Round
NA
FDA UDI
STRYKER CORPORATION·04546540374318·6.0mm X-Coarse Diamond
NA
FDA UDI
STRYKER CORPORATION·04546540346087·6.0mm XX-Coarse Diamond Round
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS·Product code JAA·March 1, 2013
ASR ACETABULER IMPLANT 56
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·February 24, 2011
NONE
FDA Adverse Event
Death
·EDWARDS LIFESCIENCES·Product code LWR·March 14, 2008
SCREW,FIXATION,BONE
FDA Adverse Event
Injury
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HWC·December 10, 2018
PLATE,FIXATION,BONE
FDA Adverse Event
Injury
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HRS·December 10, 2018