7 results
·
20ms
·
Sources: EU EUDAMED, US FDA
HPD TUBING CONNECTORS
FDA 510(k)
FDA Class 2
·Cardiovascular
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756653220·KNEE ARTHROSCOPY PACK
RESPIRONICS SEALEASY II
FDA 510(k)
FDA Class 1
·Anesthesiology
DISPOSABLE LATEX EXAM GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·June 25, 2014
PROMOTE PLUS CRT-D
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·November 10, 2010
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·January 3, 2013