10,000 results
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57ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BoneFoam
FDA UDI
BONE FOAM, INC.·00810075280722·Edema Reduction Leg Elevator Deluxe
BoneFoam
FDA UDI
BONE FOAM, INC.·00810075280739·Edema Reduction Leg Elevator Twin
BoneFoam
FDA UDI
BONE FOAM, INC.·00810075280685·Edema Reduction Leg Elevator Pediatric - Box 4
BoneFoam
FDA UDI
BONE FOAM, INC.·00810075280678·Edema Reduction Leg Elevator Large - Box of 3
Audina
FDA UDI
Audina Hearing Instruments, Inc.·00810126191397·AUDINA INSTAFIT I2 ER L
BoneFoam
FDA UDI
BONE FOAM, INC.·00810075280692·Leg Buddy Heel Cut | Box of 3
BoneFoam
FDA UDI
BONE FOAM, INC.·00810075280661·Leg Buddy | Box of 3
BoneFoam
FDA UDI
BONE FOAM, INC.·00810075280746·Edema Reduction Leg Elevator Twin Deluxe
SURESTEP
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CGA·December 9, 1998
XPS® HANDPIECE - VISAO®
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code ERL·December 9, 2015
SURESTEP
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CGA·November 10, 1998
SURESTEP
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CGA·April 6, 1999
SURESTEP
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code CGA·December 9, 1998
SURESTEP
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code CFR·February 4, 1999
DRILL, SURGICAL, ENT (PNEUMATIC) - HANDPIECE, PRODUCT CODE: ERL
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code ERL·August 28, 2013
FREESTYLE
FDA Adverse Event
Malfunction
·THERASENSE, INC.·Product code LFR·March 8, 2002
SURESTEP
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code CGA·March 2, 1999
SURESTEP
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CGA·December 9, 1998
90° CONTRA ANGLE ATTACHMENT
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HBC·October 15, 2014
DRILL/BURR ATTACHMENT FOR 2.35MM SHAFTS
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HWE·May 29, 2013