12 results
·
17ms
·
Sources: EU EUDAMED, US FDA
LENSONIC(TM) CONTACT LENS CARE ACCESSORY
FDA 510(k)
FDA Class 2
·Ophthalmic
PAQ.216X280X500/QT-HS/NK FQS216-6A-280
FDA UDI
AB MEDICA GROUP, S.A.·08428763010265·
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471121942·K-WIRE - DOUBLE TROCAR 1.1mm DIA x 125mm
Paragon 28
FDA UDI
Provision·B504OMP9919216150·
Multi System
FDA UDI
Paragon 28, Inc.·00889795152961·P28, K-Wire, 1.6 x 150 mm, Single Trocar, SMOOT...
HammerTube System
FDA UDI
Paragon 28, Inc.·00889795153265·K-Wire, Double Ended Trocar Tip, 1.6mm x 150mm
Small Bone Phantom Intramedullary Nail System
FDA UDI
Paragon 28, Inc.·00889795049735·1.6, Double-Blunt K-wire, 150 mm
4CIS VANE SPINE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
BAXTER ACCURA SYSTEM, MODEL 5M5660
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
THERASPHERE
FDA Adverse Event
Death
·MDS NORDION·Product code NAW·January 15, 2013
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code NEK·December 13, 2010
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORP·Product code FRN·February 6, 2014