130 results
·
20ms
·
Sources: EU EUDAMED, US FDA
MYOTRACK, MODEL HH 515
FDA 510(k)
FDA Class 2
·Anesthesiology
SUTURE LARIAT
FDA UDI
Biomet Orthopedics, LLC·00880304507036·
Solstice Occipito-Cervico-Thoracic System
FDA UDI
Life Spine, Inc.·00190837014599·
STILLE Forceps
FDA UDI
Stille AB·07332339202194·STILLE DRESSING FORCEPS rounded points 25 cm 10 in
SPLITTABLE SHEATH INTRODUCER KIT
FDA 510(k)
FDA Class 2
·Cardiovascular
CRESCENT SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
CRESCENT SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MSD DEGGENDORF MFG·Product code MAX·November 24, 2016
CRESCENT SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK DEGGENDORF GMBH·Product code MAX·August 19, 2011
CRESCENT SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MSD DEGGENDORF MFG·Product code MAX·January 5, 2012
CRESCENT SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MSD DEGGENDORF MFG·Product code MAX·January 13, 2012
CRESCENT SYSTEM
FDA Adverse Event
Malfunction
·MSD DEGGENDORF MFG·Product code MAX·February 2, 2012
CRESCENT SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MSD DEGGENDORF MFG·Product code MAX·July 1, 2018
CRESCENT SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MSD DEGGENDORF MFG·Product code MAX·September 6, 2016
CRESCENT SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MSD DEGGENDORF MFG·Product code MAX·May 19, 2017
CRESCENT SPINAL SYSTEM
FDA Adverse Event
Malfunction
·SOFAMOR DANEK DEGGENDORF GMBH·Product code MQP·September 23, 2010
ACCU-CHEK ® AVIVA TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·January 9, 2013
*
FDA Adverse Event
Malfunction
·SYNTHES·Product code HXL·October 18, 2010
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 1, 2014
CRESCENT SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MSD DEGGENDORF MFG·Product code MAX·December 3, 2014
CRESCENT SPINAL SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK DEGGENDORF GMBH·Product code MAX·September 8, 2011