8 results
·
18ms
·
Sources: EU EUDAMED, US FDA
LUBRIGLIDE
FDA 510(k)
FDA Class 1
·General Hospital
Edge™ Carbides FG 557 Operative Carbide Bur Sample
FDA UDI
CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172010450·Dental surgical bur
EEG NEUROAMP, MODEL CS10137
FDA 510(k)
FDA Class 2
·Neurology
MENTOR BLACK LIGHT URETERAL STENT SET
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
ENDOPATH THORACIC ENDO LINEAR CUTTER W/SAFETY LOCK
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.·Product code GAG·June 12, 1997
EON
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·February 19, 2013
TERUMO VIRTUOSAPH VEIN HARVESTING SYSTEM
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code GCJ·January 19, 2011
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·August 1, 2014