275 results
·
25ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Passio Pump Drainage System
FDA 510(k)
FDA Class 2
·Cardiovascular
LOJIC+
FDA UDI
SDI LIMITED·09336472001513·LOJIC+ 1SP SLOW 50
LOJIC+
FDA UDI
SDI LIMITED·DO3642014042·
Zodiac
FDA UDI
ALPHATEC SPINE, INC.·00844856002500·PRE CONTOURED CP ROD 5.5 x 4cm NON-BROACHED
NA
FDA UDI
Stryker GmbH·07613154639571·Screw Marker 14,4
ABSORBENT PAPER POINTS
FDA UDI
DiaDent Group International·08806383556255·"An absorbent paper points is an endodontic pap...
ORISE ProKnife
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
GOLD TOTAL AND PARTIAL, REGULAR AND OFFSET, OSSICULAR REPLACEMENT PROSTHESES, GOLD TOTAL WITH FOUNTIAN HEAD, GOLD PISTON
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
TRUERESULT
FDA Adverse Event
Malfunction
·NIPRO DIAGNOSTICS, INC.·Product code NBW·December 24, 2014
CAPSUREFIX NOVUS
FDA Adverse Event
Injury
·MPRI·Product code DTB·August 8, 2014
IFUSE IMPLANT SYSTEM
FDA Adverse Event
Injury
·SI-BONE, INC.·Product code OUR·November 4, 2019
ROTAFLOW SPANISH EU-PLUG ICU
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTQ·April 14, 2015
IFUSE IMPLANT SYSTEM
FDA Adverse Event
Injury
·SI-BONE, INC.·Product code OUR·December 7, 2017
TRUERESULT
FDA Adverse Event
Malfunction
·NIPRO DIAGNOSTICS, INC.·Product code NBW·December 24, 2014
IFUSE IMPLANT SYSTEM
FDA Adverse Event
Injury
·SI-BONE, INC.·Product code OUR·May 6, 2015
GRANUFLO
FDA Adverse Event
Death
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·June 11, 2014
RAPIDPOINT 405
FDA Adverse Event
SIEMENS HEALTHCARE DIAGNOSTICS·Product code GKR·April 23, 2015
IFUSE IMPLANT SYSTEM
FDA Adverse Event
Injury
·SI-BONE, INC.·Product code OUR·May 7, 2019
OT VERIO PRO METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 27, 2014
ACUVUE 2 BRAND CONTACT LENSES
FDA Adverse Event
Injury
·VISTAKON·Product code LPL·June 28, 2013