8 results
·
33ms
·
Sources: EU EUDAMED, US FDA
TEK-PRO TEK-TATOR V ROTATOR & HUMIDIFY
FDA 510(k)
FDA Class 1
·Microbiology
NAR
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209117581·
FEMORAL JIG SHEATH
FDA UDI
Biomet Orthopedics, LLC·00887868047855·
4.0 MM ARTHREX BIO-TENDOESIS SCREW, MODEL AR-1540B; 5.5 MM ARTHREX BIO-TENODESIS SCREW, MODELS AR-1555B
FDA 510(k)
FDA Class 2
·Orthopedic
CSM INTERNAL-R IMPLANT SYSTEM
FDA 510(k)
FDA Class 2
·Dental
SENSORMEDICS
FDA Adverse Event
Malfunction
·CAREFUSION·Product code LSZ·April 28, 2014
MECHANICAL (MANUAL) WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code IOR·November 5, 2012
LAP-BAND AP ADJUSTABLE GASTRIC BANDING SYSTEM (STANDARD)
FDA Adverse Event
Malfunction
·ALLERGAN·Product code LTI·August 24, 2010