25 results
·
25ms
·
Sources: EU EUDAMED, US FDA
EARSCOPE
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
SureStep™ Foley Tray System Bard® Lubricath Foley
FDA UDI
C. R. Bard, Inc.·00801741073960·SureStep® Foley Tray System Bard® Lubricath® Fo...
MGB Alert Internal Control Set MS2-E
FDA UDI
Elitechgroup Mdx LLC·03661540951442·The MGB Alert Internal Control Set MS2-E consis...
Bard® Urine Meter Foley Catheter Tray With Bard® Hydrophilic-Coated Foley
FDA UDI
C. R. Bard, Inc.·00801741020124·Bard® Urine Meter Foley Catheter Tray With Bard...
NAR Kit
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209101528·KIT, RESCUE TASK FORCE VEST w' SIDE ARMOR - BLK
Elite Orthopaedics
FDA UDI
Elite Orthopaedics, Inc.·00816591013998·OA Knee Brace, Single Upright, Right
ACUMED
FDA UDI
Acumed LLC·10806378041570·Lkg RH Tray Insert Base
AcQMap®
FDA UDI
ACUTUS MEDICAL, INC.·00857042007210·Patient Electrode Kit 900100
Marina Medical
FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306810176·Hoyos 3-Hole Harvester, 9G x 30cm, 60cc
Elite Orthopaedics
FDA UDI
Elite Orthopaedics, Inc.·00816591014001·OA Knee Brace, Single Upright, Left
AcQMap
FDA UDI
ACUTUS MEDICAL, INC.·00857042007036·AcQMap® Patient Electrode Kit
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197491440·Titanium Blade
51x102...
Marina Medical
FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306835421·Pre-Assembled 3-Hole Hoyos Harvester, 09GA X 30...
MORCE POWER PLUS AND VARIOCARVE MORCELLATOR
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
ACCU-CHEK ADVANTAGE METER
FDA 510(k)
FDA Class 2
·Clinical Chemistry
BARD® LUBRICATH® FOLEY CATHETER
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZC·June 6, 2019
Catalog A800365, SureStep" Foley Tray, Bard LubricathTM Foley Catheter Tray
FDA Enforcement
Class II
·Ongoing·C.R. Bard Inc·September 29, 2021
UNKNOWN- UNSPECIFIED BY COMPLAINANT
FDA Adverse Event
Injury
·COOK BIOTECH, INC.·Product code FTM·April 3, 2014
ACCU-CHEK ® AVIVA PLUS TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·October 22, 2012
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC, USA·Product code LFR·September 28, 2007