16 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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EchoPAC Software Only, EchoPAC Plug-In
FDA 510(k)
FDA Class 2
·Radiology
OsteoMed
FDA UDI
OSTEOMED LLC·00845694057226·Trocar, Long Cannula, ICON
RENEW NEUROSTIMULATION SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
POLY-CHEM GLUCOSE
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Widex
FDA UDI
Widex A/S·05706069724905·Widex D-CIC (Dark brown S-330 ) Left, RC coil
Widex
FDA UDI
Widex A/S·05706069726466·Widex mind330 M3-X ITE (Dark brown S-330 ) Tele...
Widex
FDA UDI
Widex A/S·05706069725261·Widex EVOKE E-IP (Dark brown S-330 ) Right
Widex
FDA UDI
Widex A/S·05706069725865·Widex EVOKE E-CIC (Dark brown S-330 ) Left, RC ...
Widex
FDA UDI
Widex A/S·05706069724547·Widex UNIQUE U-CIC L (Dark brown S-330 ) Left, ...
DUOVISC VISCOELASTIC SYSTEM
FDA Adverse Event
Injury
·ALCON - COUVREUR N.V./ALCON - BELGIUM·Product code LZP·October 29, 2022
PROVISC OPHTHALMIC VISCOSURGICAL DEVICE
FDA Adverse Event
Injury
·ALCON - COUVREUR N.V./ALCON - BELGIUM·Product code LZP·October 29, 2022
VISCOAT OPHTHALMIC VISCOSURGICAL DEVICE
FDA Adverse Event
Injury
·ALCON - COUVREUR N.V./ALCON - BELGIUM·Product code LZP·October 29, 2022
COLLEAGUE 3 VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 20, 2008
INTERSTIM II
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code EZW·August 8, 2011
GYNECARE TVT RETROPUBIC SYSTEM
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTN·July 2, 2013
APEX MODULAR HIP STEM
FDA Adverse Event
Injury
·OMN LIFE SCIENCE, INC.·Product code KWY·May 28, 2008