17 results
·
27ms
·
Sources: EU EUDAMED, US FDA
FLEXIBLE IMMERSIBLE SIGMOIDOSCOPE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Bard® Center Entry Urine Meter Add-A-Foley Tray with Bard EZ-Lok® Sampling Port
FDA UDI
C. R. Bard, Inc.·00801741029097·Bard® Center Entry Urine Meter Add-A-Foley Tray...
Greenwald Surgical Company, Inc.
FDA UDI
GRACE MANUFACTURING, INC.·10801334006983·BOVIE UNIVERSAL ADAPTER
IMA Super-Slide Retractor Set
FDA UDI
KOROS U.S.A., INC.·10840199544612·IMA Super-Slide Retractor Set Consists of the F...
ZAVATION
FDA UDI
Zavation LLC·00197157014896·TIGER 2 X-TAB DILATION TUBE #2
ZAVATION DILATION TUBE
FDA UDI
Zavation LLC·00197157014889·TIGER 2 X-TAB DILATION TUBE #1
ZAVATION DILATION TUBE
FDA UDI
Zavation LLC·00197157014902·TIGER 2 X-TAB DILATION TUBE #3
POWDER-FREE, YELLOW VINYL PATIENT EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
D R Burton OxyPAP
FDA 510(k)
FDA Class 2
·Anesthesiology
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·June 24, 2014
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·July 6, 2015
MECHANICAL CHAIR/TRANSPORT CHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code INM·January 1, 2013
COMPREHENSIVE REVERSE SHOULDER GLENOSPHERE 36MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code PAO·April 27, 2017
COMPREHENSIVE REVERSE SHOULDER HUMERAL BEARING STANDARD +3MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code PAO·April 27, 2017
COMPREHENSIVE REVERSE SHOULDER HUMERAL TRAY 44MM STANDARD
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWS·April 27, 2017
BIOMET StageOne Knee Tibial Cement Spacer Mold, 80 MM, Silicone, Sterile, Item 433180.
FDA Enforcement
Class II
·Terminated·Biomet, Inc.·April 15, 2020
OEC 9800; OEC FluoroTrak 9800 Plus; OEC 9800 Plus; OEC 9800 MD Motorized C-arm System, 892.1650 Image-intensified fluoroscopic x-ray system. The OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical and interventional procedures. The system includes features specifically designed for use in diagnostic and interventional cardiac imaging procedures and is also intended for cholangiography, endoscopic, urologic orthopedic, neurologic, vascular, critical care and emergency room procedures. It may be used for other imaging applications at the physician's discretion.
FDA Enforcement
Class I
·Terminated·GE OEC Medical Systems, Inc·August 1, 2012