22 results
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38ms
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Sources: EU EUDAMED, US FDA
XLTEK EVOKED POTENTIAL HEADBOX, MODEL EP-4-RP (PROPOSED)
FDA 510(k)
FDA Class 2
·Neurology
Avitene
FDA UDI
Davol Inc.·00801741010460·Avitene Non-Woven Web, 70 mm x 35 mm x 1 mm
PUMA-G System™
FDA UDI
Coaptech, Inc.·10860312001532·External Magnet in Case
Batrik In-Brush Twisted Wire Brushes
FDA UDI
Batrik Medical Manufacturing Inc·00690521005594·Brush\7Fraizier\BD-2.30mm\BL-25.4mm\OL-250mm - ...
Santis Pre Bent Rod 5.5mmx90mm
FDA UDI
Lanterna Medical Technologies GmbH·07640159550648·Santis Pre Bent Rod 5.5mmx90mm
SANTIS™ PRE BENT ROD 5.5mm X90mm -STERILE
FDA UDI
Lanterna Medical Technologies GmbH·07640159551768·SANTIS™ PRE BENT ROD 5.5mm X90mm -STERILE
Integrity-SI Fusion System
FDA UDI
Lincotek Medical LLC·B57112521010090D0·10 x 90 mm Anodized SI Implant
mahe medical GmbH
FDA UDI
mahe medical gmbh·04050659173415·6.5 Cancellous Bone Shaft Screw, hex, _x000D_...
GMA 2.0 Pedicle Screw System
FDA UDI
GRAFTON MEDICAL ALLIANCE, INC.·00810021380292·PRE-BENT ROD, ø5.5 X 90
6.5 Cancellous Bone Shaft Screw, hex, St.Steel, L 90/16 mm
FDA UDI
mahe medical gmbh·EMAH00100100900·6.5 Cancellous Bone Shaft Screw, hex,
St.Ste...
METHAFILCON A
FDA 510(k)
FDA Class 2
·Ophthalmic
GUTHRIE PRIME POWDER-FREE CHLORINATED PATIENT EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
SEE H10
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code NBC·April 18, 2013
MEDSTONE LITHOTRIPTOR
FDA Adverse Event
Malfunction
·HEALTHTRONICS, INC.·Product code LNS·June 12, 2017
ACIST
FDA Adverse Event
Injury
·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·February 10, 2012
AXSYM DIGOXIN III
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS INTERNATIONAL, LTD.·Product code KXT·May 11, 2007
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 19, 2013
ACCU-CHEK ® COMFORT CURVE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·March 8, 2011
ACIST
FDA Adverse Event
Malfunction
·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·April 20, 2007
ACIST
FDA Adverse Event
Injury
·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·February 10, 2012