255 results
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23ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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GLASS LOSS OF RESISTANCE SYRINGE
FDA 510(k)
FDA Class 2
·Anesthesiology
SOLIDEA
FDA UDI
CALZIFICIO PINELLI SRL·08300496063018·SOCKS FOR YOU BAMBOO OPERA, SIZE XL, GRIGIO, GR...
Bausch + Lomb
FDA UDI
Bausch & Lomb Incorporated·00757770425655·eXTRA TIP FOR N-630 18 GAUGE
Sterilance Press2 Disposable Safety Lancet
FDA UDI
Sterilance Medical (Suzhou) Inc.·16945630115087·
STERiLANCE Press2 Disposable Safety Lancet
FDA UDI
Sterilance Medical (Suzhou) Inc.·16945630131087·
Sterilance Press2 Pressure Activated Safety Lancet
FDA UDI
Sterilance Medical (Suzhou) Inc.·16945630109932·Sterilance Press2 Pressure Activated Safety Lan...
General Instruments
FDA UDI
ALPHATEC SPINE, INC.·00840180501337·Medial/Lateral Angled LIF Cobb - 18MM, RIGHT
General Instruments
FDA UDI
ALPHATEC SPINE, INC.·00840180501320·Medial/Lateral Angled LIF Cobb - 18MM, LEFT
TITAN TIBIAL NAIL
FDA 510(k)
FDA Class 2
·Orthopedic
REAADS ANTI-PHOSPHATIDYLSERINE IGA SEMI-QUANTITIVE TEST KIT
FDA 510(k)
FDA Class 2
·Immunology
ZILVER 635 SELF-EXPANDING BILIARY STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·August 29, 2022
ZILVER 635 BILIARY SELF EXPANDING METAL STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·October 8, 2020
ZILVER 635 BILIARY SELF EXPANDING METAL STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·May 20, 2022
ZILVER 635 BILIARY SELF EXPANDING METAL STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·June 26, 2024
ZILVER 635 BILIARY SELF EXPANDING METAL STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·July 1, 2020
ZILVER 635 BILIARY SELF EXPANDING METAL STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·January 17, 2022
ZILVER 635 BILIARY SELF EXPANDING METAL STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code NIU·November 8, 2019
AUTOPULSE RESUSCITATION SYSTEM MODEL 100
FDA Adverse Event
Malfunction
·ZOLL CIRCULATION, INC.·Product code DRM·March 26, 2013
INTEGRIS H5000F/ALLURA 9F
FDA Adverse Event
Malfunction
·PHILIPS HEALTHCARE·Product code IZI·March 21, 2011
MANUAL ORTHOPEDIC SURGICAL INSTRUMENT
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code LXH·June 19, 2008