10 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Béa Applicator (BAP-GB-01)
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
NA
FDA UDI
Medos International Sàrl·10886705031634·Sheath with 1 Rotating Stopcock compatible wit...
n/a
FDA UDI
Hager & Meisinger Gesellschaft mit beschränkter Haftung·E0HM59002421070311·Rotary instrument for ENT surgery
OPUS SPEEDSTITCH SUTURE DEVICE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Talent-Pro Electromagnetic Stimulator
FDA 510(k)
FDA Class 2
·Physical Medicine
BD PRECISIONGLIDE NEEDLE
FDA Adverse Event
Malfunction
·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·June 19, 2020
GREEN LIGHT PV
FDA Adverse Event
Malfunction
·AMERICAN MEDICAL SYSTEMS, INC.·Product code GEX·November 17, 2008
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·COCHLEAR LTD.·Product code MCM·September 9, 2011
OT VERIO PRO METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2013
BD PRECISIONGLIDE¿ NEEDLE
FDA Adverse Event
Malfunction
·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·March 17, 2020