12 results
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30ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CD HORIZON SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code KWP·November 7, 2019
Biomet® Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304232259·
Novo Surgical
FDA UDI
NOVO SURGICAL, INC.·G586G1414940·operating scissors, blunt/blunt, curved, slende...
HANDHELD PULSE OXIMETER
FDA 510(k)
FDA Class 2
·Cardiovascular
OLYMPUS INTEGRATED ENDOSURGERY SYSTEM ENDOALPHA (CONTROL UNIT FOR ENDOSURGERY UCES-2) SOFTWARE VERSION 2
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MECHANICAL CHAIR/TRANSPORT CHAIR
FDA Adverse Event
Malfunction
·GOODBABY·Product code INM·May 10, 2012
KOTEX NATURAL BALANCE : TAMPON, MENSTRUAL, UNSCENTED : HEB
FDA Adverse Event
Malfunction
·KIMBERLY-CLARK CORPORATION CONWAY MILL·Product code HEB·June 21, 2018
MECHANICAL CHAIR/TRANSPORT CHAIR
FDA Adverse Event
GOODBABY·Product code INM·July 24, 2012
RETAINING STEM INSERTER
FDA Adverse Event
Malfunction
·1818910 DEPUY ORTHOPAEDICS, INC.·Product code LXH·October 4, 2014
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013
DEPUY ASR XL FEM IMP SIZE 49
FDA Adverse Event
Injury
·DEPUY INTERNATIONL, LTD.·Product code KWA·June 22, 2011