28 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
SOFTRANS INTRAUTERINE PRESSURE CATHETER SYSTEM (IUP 4000 SOFTRANS IUPC)
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
SPACELABS MODEL 90419 PULSE OXIMETER MODULE
FDA 510(k)
FDA Class 2
·Cardiovascular
PAROJECT ANESTHETIC SYRINGE
FDA 510(k)
FDA Class 2
·Dental
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·June 3, 2019
TSRH
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·July 11, 2017
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·February 10, 2017
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·January 9, 2017
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·June 12, 2020
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·June 12, 2020
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·July 22, 2016
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·October 6, 2016
46 ELEV.
FDA Adverse Event
Malfunction
·INTEGRA YORK, PA INC.·Product code GEN·June 19, 2014
UNIVERSAL HANDPIECE
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS-KALAMAZOO·Product code LFL·February 15, 2013
ACCU-CHEK ® MULTICLIX
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code FMK·January 19, 2011
TSRH
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·October 7, 2011
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·July 22, 2016
TSRH
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·October 12, 2018
TSRH
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·March 15, 2017
TSRH
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·May 14, 2017
TSRH
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·May 23, 2017