11 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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Site~Rite Halcyon Diagnostic Ultrasound System
FDA 510(k)
FDA Class 2
·Radiology
SILICONE PIP
FDA UDI
Stryker GmbH·00886385021355·Broach, Proximal, Size 50
BD DISCARDIT II SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMF·October 1, 2021
SKIN CARE LIGHT
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
APLIO DIAGNOSTIC ULTRASOUND SYSTEM; APLIO DIAGNOSTIC ULTRASOUND SYSTEM; APLIO DIAGNOSTIC ULTRASOUND SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
BD INSYTE¿ AUTOGUARD¿ SHIELDED IV CATHETER
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·December 16, 2019
BD INSYTE AUTOGUARD SHIELDED IV CATHETER
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·June 3, 2020
HEART START XL
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·May 23, 2013
ACCU-CHEK SPIRIT
FDA Adverse Event
Malfunction
·ROCHE INSULIN DELIVERY SYSTEMS, INC.·Product code LZG·June 22, 2011
COLLEAGUE 3 VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·September 24, 2008
ANALYTICAL E MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code DHA·October 4, 2013