26 results
·
18ms
·
Sources: EU EUDAMED, US FDA
JOSTRA MECC SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776177812·Hegar Dilator fr
Conmed/Linvatec
FDA UDI
Provision·00810041065650·
Conmed/Linvatec
FDA UDI
Provision·B504OM50231320·
Reprocessed Micro Choice Sagittal Blade, Coarse, 5.5 x 25.5mm
FDA UDI
SURETEK MEDICAL·B39050231321·
CONMED
FDA UDI
Conmed Corporation·10845854009550·MICRO SAGITTAL BLADE, COARSE, 5.5 X 25.5 X 0.4 MM
NA
FDA UDI
STERILMED, INC.·10888551017763·SAW BLADE MICRO SAGITTAL
NA
FDA UDI
STERILMED, INC.·10888551019699·SAW BLADE SAGITTAL COARSE TOOTH
SIGN IM NAIL
FDA 510(k)
FDA Class 2
·Orthopedic
DERMAGRIP POWDER FREE BLUE POLYMER COATED LATEX EXAMINATION GLOVE, NON-STERILE CONTAINS 50 MICROGRAM OR LESS OF TOTAL WA
FDA 510(k)
FDA Class 1
·General Hospital
AXIOS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 2, 2024
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCOR...·Product code CBK·February 27, 2013
STENOSCOP
FDA Adverse Event
Malfunction
·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD (GE PRIVATE)·Product code JAA·February 24, 2011
COLLEAGUE CX VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·April 3, 2008
VUELOCK SCREW, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code KWQ·April 16, 2020
VEULOCK SCREW, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code KWQ·April 16, 2020
VEULOCK SCREW, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code KWQ·April 16, 2020
VEULOCK SCREW, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code KWQ·April 16, 2020
HOSP SS FLEXX METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·May 12, 2011
HOSP SS FLEXX METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·May 12, 2011