12 results
·
24ms
·
Sources: EU EUDAMED, US FDA
OLYMPUS MAJ-172 INSTRUMENT TRAY FOR LTF VIDEOSCOPE
FDA 510(k)
FDA Class 2
·General Hospital
ArgenZ HT+ 95x30 C1
FDA UDI
ARGEN CORPORATION, THE·D818122818·Dental porcelain/ceramic restoration kit
MICRUS ONE 2 ONE GUIDEWIRE, MICRUS ONE 2 ONE SOFT GUIDEWIRE
FDA 510(k)
FDA Class 2
·Cardiovascular
MULTIPLE, BLUE POWDER FREE NITRILE EXAMINATION GLOVES WITH PEPPERMINT FLAVOR
FDA 510(k)
FDA Class 1
·General Hospital
VERCISE CARTESIA
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code PJS·December 18, 2024
IOLMASTER 500
FDA Adverse Event
Malfunction
·CARL ZEISS MEDITEC AG (JENA)·Product code HJO·October 14, 2015
UNICEL® DXL 600 ACCESS® IMMUNOASSAY SYSTEM
FDA Adverse Event
Injury
·BECKMAN COULTER, INC.·Product code MMI·June 25, 2012
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·May 21, 2013
4580 FMS DUO+ PUMP/SHAVER COMBO
FDA Adverse Event
Injury
·DEPUY MITEK·Product code HRX·September 26, 2014
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 14, 2011
ACCESS 2 IMMUNOASSAY SYSTEM
FDA Adverse Event
Injury
·BECKMAN COULTER, INC.·Product code MMI·June 25, 2012
SYNCHRON LXI 725 SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code MMI·August 9, 2012