12 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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SURGITEK(R) LUBRI-FLEX(TM) URETERAL STENT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
TRU/PUR 3.0mm Drill 6,8,10,12,14mm
FDA UDI
STERNGOLD DENTAL LLC·00841549114816·A metal device used in dental surgery to create...
IMMULITE® 2000 Xpi Sample Nesting Cups
FDA UDI
SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD·00630414982410·Test tube, non-sterile
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471122796·K-WIRE - SINGLE TROCAR THREADED 2.8mm DIA x 230mm
MRT 50A 100MM CIRCULAR SURFACE COIL
FDA 510(k)
FDA Class 2
·Radiology
RONGEUR, ORTHOPEDIC SURGICAL INSTRUMENTS
FDA 510(k)
FDA Class 1
·Orthopedic
QUARTET
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·January 9, 2013
FLO-GARD 6201 VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·November 22, 2010
TELIGEN
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 1, 2014
BD 20 ML SYRINGE WITH NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·August 6, 2020
SYRINGE S2 20ML 18GA 1-1/2IN BD CHINA
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·November 24, 2020
SYRINGE S2 20ML 18GA 1-1/2IN BD CHINA
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·November 25, 2020