9 results
·
26ms
·
Sources: EU EUDAMED, US FDA
THE 3500
FDA 510(k)
FDA Class 2
·Neurology
Tranquil-C™
FDA UDI
NEXUS SPINE, L.L.C.·B6788223960·Cervical Rasp + DS 9x18x14 Flat
POWERED VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)
FDA 510(k)
FDA Class 1
·General Hospital
GENERAL PROCEDURE AGAROSE FILM
FDA 510(k)
FDA Class 1
·Clinical Chemistry
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·May 20, 2014
SEVEN CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·November 7, 2012
ULTRACISION HARMONIC SCALPEL CURVED SHEARS (LCS) - PISTOL GRIP 36 CM - 15 MM ACT
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC (CINCINNATI)·Product code GEI·August 17, 2007
ARCOS TROCHANTERIC CLAW
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·April 17, 2018
FEMORAL LOCKING SCREW
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·April 17, 2018