196 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Medline Powder-Free Orange Nitrile Patient Examination Glove (Tested for use with Fentanyl)
FDA 510(k)
FDA Class 1
·General Hospital
GERALD TISSUE FORCEPS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896060241·GERALD TISSUE FORCEPS DEBAKEY TIP
Drill
FDA UDI
Treace Medical Concepts, Inc.·00810111222433·Drill
PurCel Labs Small Vinyl Exam Gloves
FDA UDI
Purcel Labs LLC·00810143550221·Clear Vinyl Exam Gloves, Size Small, Medical Gr...
Golden Isles Pedicle Screw System
FDA UDI
Intelivation, LLC·G079C2522001500·Straight Titanium Rod
TAURUS
FDA UDI
CTL Medical Corporation·00841732163690·Taurus Pedicle Screw System- Straight Rod 5.5x1...
Taurus Pedicle Screw System
FDA UDI
SINTX Technologies, Inc.·M555252200150·Taurus Pedicle Screw System- Straight Rod 5.5x1...
CorticaLINK MI
FDA UDI
LINKSPINE, INC.·00817329023173·5.0mm Cobalt Chrome Rod: 150mm Curved
Preference 2
FDA UDI
SINTX Technologies, Inc.·M555102200150·Straight Rod 6.0mm, 150mm
CERAMICS2IN1
FDA 510(k)
FDA Class 2
·Dental
CRC-15BT
FDA 510(k)
FDA Class 2
·Radiology
INTERMEDIATE DRILL
FDA UDI
SWEDEN & MARTINA SPA·D7701348693·INTERMEDIATE DRILL SLEEVE 415 D.2.00 L.15.00 MM
DRILL
FDA UDI
SWEDEN & MARTINA SPA·D7702694133·DRILL SLEEVE 5.0 D.2.00 L.15.0 MM
INTERMEDIATE DRILL
FDA UDI
SWEDEN & MARTINA SPA·D7701349113·INTERMEDIATE DRILL SLEEVE 550 D.2.00 L.15.00 MM
BIOGX SARS-COV-2 OPEN SYSTEM REAGENTS FOR BD MAX SYSTEM
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code QJR·August 5, 2020
FASTTAKE
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CFR·April 26, 2002
ONE TOUCH ULTRA
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CFR·September 5, 2002
ONE TOUCH II
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CFR·August 7, 2002
ONE TOUCH BASIC ENHANCED
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CFR·July 26, 2002
SURESTEP
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CGA·June 25, 1999