26 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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SYNTHES LARGE EXTERNAL FIXATION, MR CONDITIONAL
FDA 510(k)
FDA Class 2
·Orthopedic
LARGE EX-FIX COMBINATION CLAMP MR-CONDITIONAL
FDA Adverse Event
Injury
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code KTT·April 12, 2018
SELDRILL-SCHANZSCR Ø5 L200/80 SST
FDA Adverse Event
Injury
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code KTT·April 12, 2018
LARGE EX-FIX 11MM CRBN FBR ROD 250MM / MR-CONDITIONAL
FDA Adverse Event
Injury
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code KTT·April 12, 2018
LARGE EX-FIX 11MM CRBN FBR ROD 300MM / MR-CONDITIONAL
FDA Adverse Event
Injury
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code KTT·April 12, 2018
SELDRILL-SCHANZSCR Ø5 L200/80 SST
FDA Adverse Event
Injury
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code KTT·April 12, 2018
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16740826500·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1674082650060·
Therapy Interface Tubing kit
FDA UDI
Respironics, Inc.·00606959052055·Therapy Interface Tubing Kit
Zavation
FDA UDI
Zavation LLC·00842166149762·8x26x50mm, 0°, MILC
Centaur Pedicle Screw System
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215127015·
V60 VENTILATOR
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, INC·Product code MNT·July 9, 2015
VAN ANDLE DILATION, EMERALD GUIDEWIRE, MODEL VAD6, 502-726
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
HYGIA HEALTH SERVICES REPROCESSED NUTECH FOOT WRAP
FDA 510(k)
FDA Class 2
·Cardiovascular
V60 VENTILATOR
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, INC·Product code MNT·August 3, 2015
PAXGENE® BLOOD RNA TUBE
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code NTW·May 1, 2026
ACCU-CHEK ® AVIVA PLUS TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·April 29, 2013
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code MDS·April 27, 2011
EXPRESS VASCULAR SD
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code MAF·July 23, 2008
UNSPECIFIED BD PAXGENE® BLOOD TUBE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code PJE·June 13, 2025