396 results
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33ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Hepatitis A Test (Antibody And Igm Antibody)
FDA Pre-Market Approval
FDA Class 2
·ADVIA CENTAUR HAV TOTAL ASSAY, ADVIA CENTAUR HAV TOTAL QUALITY CONTROL MATERIALS
Leksell Vantage Stereotactic System
FDA UDI
Elekta Solutions AB·07340201501283·FirmFix™ 2
FirstPlug
FDA UDI
35newtons L.L.C.·00860005367207·FirstPlug Screw Channel Barrier 210 cm
23GA Illuminating Laser Probe, SMA906
FDA UDI
Peregrine Surgical, Llc·00632307001819·23GA Illuminating Laser Probe, SMA906
FirstPlug
FDA UDI
35newtons L.L.C.·00860005367221·FirstPlug Screw Channel Barrier 210 cm
FirstPlug
FDA UDI
35newtons L.L.C.·00860005367238·FirstPlug Screw Channel Barrier 210 cm
FirstPlug
FDA UDI
35newtons L.L.C.·00860005367252·FirstPlug Screw Channel Barrier 210cm
Multicare Platinum
FDA UDI
Hologic, Inc.·15420045505926·
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710820400170·Zadik Calcaneal Guide, 40mm x 17°
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710310400170·Talar Osteotmy Guide, 40mm x 17mm
ABC CAUDAL AND CRANIAL EXTENSION PLATE (E-PLATE)
FDA 510(k)
FDA Class 2
·Orthopedic
INFINION CX
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·December 14, 2023
ARTICULEZE M HEAD 36MM +5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·April 8, 2013
U BY KOTEX CLICK TAMPONS
FDA Adverse Event
Malfunction
·AVENT S. DE R.L. DE C.V.·Product code HEB·March 9, 2011
EASY LOAD INSERTION DEVICE
FDA Adverse Event
Injury
·BAUSCH & LOMB·Product code MSS·May 6, 2008
BD ONCLARITY HPV ASSAY REAGENT PACK
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code MAQ·September 12, 2024
BD ONCLARITY HPV ASSAY REAGENT PACK
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code MAQ·September 12, 2024
BD ONCLARITY HPV ASSAY REAGENT PACK
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code MAQ·September 12, 2024
VERIFLEX¿
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code MAF·January 10, 2013
VERIFLEX (LIBERTE) CORONARY STENT DELIVERY SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - GALWAY·Product code MAF·June 17, 2010