21 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Biopsy Forceps
FDA 510(k)
FDA Class 2
·Cardiovascular
APEX Revision Knee
FDA UDI
Omni Life Science, Inc.·00841690124597·Modular Offset Stem 17mm x 125mm 2mm
OsteoMed
FDA UDI
OSTEOMED LLC·00845694018548·MFx 2.7mm x 22mm Angulated Locking Safety Screw
neoV980 & neoV1470 Diode Lasers
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
LIFESHIELD LATEX-FREE MICROBORE EXTENSION SET, MODEL 14949 AND OTHERS
FDA 510(k)
FDA Class 2
·General Hospital
EXTENSION SET WITH T-CONN. SL
FDA Adverse Event
Malfunction
·HOSPIRA LTD.·Product code FPA·September 21, 2010
LS LF IV SET CONVRT PP W/BCCK VLV 2CLAVE
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FPA·April 14, 2011
LS MICROBR EXT SET
FDA Adverse Event
Malfunction
·HOSPIRA LTD.·Product code FPA·August 16, 2010
EXTENSION SET WITH T-CONN. SL
FDA Adverse Event
Malfunction
·HOSPIRA, LTD.·Product code FPA·March 15, 2012
EXTENSION SET WITH T-CONN.SL
FDA Adverse Event
Malfunction
·HOSPIRA LTD.·Product code FPA·January 21, 2010
EXTENSION SET WITH T-CONN. SL
FDA Adverse Event
Malfunction
·HOSPIRA LTD.·Product code FPA·October 14, 2011
NATURALYTE
FDA Adverse Event
Death
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·November 13, 2014
UNICEL DXC 600 SYNCHRON CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JGS·September 9, 2011
ACCU-CHEK ® AVIVA TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·July 29, 2013
EXTENSION SET WITH T-CONN.SL
FDA Adverse Event
Malfunction
·HOSPIRA LTD.·Product code FPA·January 21, 2010
LS LF IV SET CONVRT PP W/BCCK VLV 2CLAVE
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FPA·March 14, 2011
LS MICROBR EXT SET
FDA Adverse Event
Malfunction
·HOSPIRA, LTD.·Product code FPA·August 17, 2010
LS LF IV SET CONVRT PP W/BCCK VLV 2CLAVE
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FPA·December 6, 2010
LS MICROBR EXT SET
FDA Adverse Event
Malfunction
·HOSPIRA LTD.·Product code FPA·August 16, 2010
INDUO
FDA Adverse Event
Injury
·NOVO NORDISK A/S, MEDICAL SYSTEMS·Product code KZE·May 25, 2006