7 results
·
25ms
·
Sources: EU EUDAMED, US FDA
WIRE REINFORCED SILICONE ENDOTRACHEAL TUBE
FDA 510(k)
FDA Class 2
·Anesthesiology
MEDTRONIC BIO-MEDICUS BIO-CONSOLE MODEL 540-D
FDA 510(k)
FDA Class 2
·Cardiovascular
PATIENTMATE TM
FDA 510(k)
FDA Class 2
·General Hospital
SECURE ACUTE CARE BED 3/01
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FNL·February 11, 2013
UNIFY CRT-D, DF-4 CONNECTOR
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·January 10, 2011
TAPERLOC POR FMRL LAT 13.5X147
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LPH·July 24, 2014
BARD Dynamic Tip Steerable, Product Number 6DYNTP001;
FDA Enforcement
Class II
·Ongoing·Stryker Sustainability Solutions·May 20, 2026