23 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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APTUS® Proximal Humerus System
FDA 510(k)
FDA Class 2
·Orthopedic
LoFric® Elle™
FDA UDI
Wellspect AB·07333387024530·Single Use Urinary Catheter LoFric Elle Nelaton...
LoFric® Elle™
FDA UDI
Wellspect AB·07392532235429·Single Use Urinary Catheter LoFric Elle Nelaton...
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X1814250·18mm x 14mm W x 25mm L x 0 degrees XLIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X18142580·18mm H x 14mm W x 25mm L x 8 degrees XLIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X181425120·18mm H x 14mm W x 25mm L x 12 degrees XLIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587L181425120·18mm H x 14mm W x 25mm L XLIF Trial 12 degree L...
Origin 125º Short Neck Hip Stem
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215024079·
Best Medical International
FDA UDI
BEST MEDICAL INTERNATIONAL, INC.·00841365103926·
MICROSCAN DRIED GRAM-NEGATIVE MIC/COMBO PANEL, B1017 PANEL SERIES
FDA 510(k)
FDA Class 2
·Microbiology
COOK VASCULAR INC. VITAL-PORT VASCULAR ACCESS SYSTEM POWER INJECTABLE PORT
FDA 510(k)
FDA Class 2
·General Hospital
CART 9733856 S7 STAFF ASSEMBLED 110V
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC·Product code HAW·June 4, 2019
VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT
FDA Adverse Event
Injury
·COOK VASCULAR INC·Product code LJT·November 4, 2015
STEALTHSTATION® S7´
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC·Product code HAW·June 20, 2019
CART 9733856 S7 STAFF ASSEMBLED 110V
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC·Product code HAW·June 17, 2019
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·October 17, 2014
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 27, 2011
*
FDA Adverse Event
Malfunction
·*·Product code FMF·June 17, 2013
VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT
FDA Adverse Event
Injury
·COOK VASCULAR INC·Product code LJT·November 17, 2017
BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·September 10, 2021