9 results
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19ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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KARL STORZ NASAL,, TONSIL, EAR, LARYNGEAL SNARE
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
Irrigation Tip
FDA UDI
DiaDent Group International·08806383562461·This device connected with manually-operated sy...
Elite® Buccal Tubes Direct Bond
FDA UDI
Ortho Organizers, Inc.·00190707074678·Elite®.018 EDGE U7R NL MINI OPTI-MIM DB
E1 MEDICAL FLAT PANEL DISPLAY SYSTEM AND MFGD 1218 MEDICAL FLAT PANEL DISPLAY
FDA 510(k)
FDA Class 2
·Radiology
Stryker ICONIX with Needles
FDA 510(k)
FDA Class 2
·Orthopedic
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 8, 2013
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·January 6, 2011
ENDOTAK RELIANCE
FDA Adverse Event
Malfunction
·CPI - DEL CARIBE·Product code NVY·July 22, 2014
Philips Azurion 7M20 systems with FlexArm ceiling-mounted system, Interventional Fluoroscopic X-Ray System, Model Numbers 722079 and 722224
FDA Enforcement
Class II
·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·September 11, 2024