15 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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QiF Blood and Fluid Warmer
FDA 510(k)
FDA Class 2
·General Hospital
LeMaitre Embolectomy Catheter
FDA UDI
Lemaitre Vascular, Inc.·00840663101054·5F 40 cm NovaSil Silicone Single Lumen Embolect...
LeMaitre Embolectomy Catheter
FDA UDI
Lemaitre Vascular, Inc.·00840663100934·5F 40 cm NovaSil Silicone Single Lumen Embolect...
Super Upper Limbs Versalock Plating System
FDA UDI
GM DOS REIS INDUSTRIA E COMERCIO LTDA·07899258695778·VERSALOCK DISTAL ULNA “L” PLATE 51.0mm, RIGHT
Super Upper Limbs Versalock Plating System
FDA UDI
GM DOS REIS INDUSTRIA E COMERCIO LTDA·07899258695785·VERSALOCK DISTAL ULNA “L” PLATE 51.0mm, LEFT
ACUITY UNIVERSAL CUTTER
FDA 510(k)
FDA Class 2
·Cardiovascular
FIXCET SPINAL FACET SCREW SYSTEM
FDA 510(k)
FDA Unclassified
·Unknown
SCRDRIVER F/EXTRACT
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code HXX·December 21, 2012
UNICEL® DXC 600 SYNCHRON® CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JJE·July 27, 2011
TOTAL CARE BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·June 4, 2013
SUMMIT DUOFIX TAP SZ7 STD OFF
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code LPH·September 26, 2008
BELIFU
FDA Adverse Event
Injury
·HONG QIANGXING (SHEN ZHEN) ELECTRONICS LIMITED·Product code GZJ·February 10, 2020
6.5MM TI HEADLESS COMPRESSION SCREW/16MM THREAD/80MM
FDA Adverse Event
Injury
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HWC·July 23, 2019
6.5MM TI HEADLESS COMPRESSION SCREW/16MM THREAD/80MM
FDA Adverse Event
Injury
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HWC·July 23, 2019
6.5MM TI HEADLESS COMPRESSION SCREW/16MM THREAD/80MM
FDA Adverse Event
Injury
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HWC·July 23, 2019