10 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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uNion Cervical Plate System
FDA 510(k)
FDA Class 2
·Orthopedic
TruLink
FDA UDI
OSI OPTOELECTRONICS, INC.·00859998006460·SpO2 Cloth Sensor Single-Patient Use - Infant
HNM Women Care
FDA UDI
HNM STAINLESS, LLC.·00812171028338·PESSARY, GEHRUNG #5, 75mm
Trulink
FDA UDI
SPACELABS HEALTHCARE (WASHINGTON), INC·10841522102370·SENSOR,SPO2,CLOTH,INFANT,SPU,24/BX,ROHS
KHAN KINETIC TREATMENT (KKT-M2)
FDA 510(k)
FDA Unclassified
·Unknown
GENEROS, MODELS GO-01G, GO-05G, GO-10G, GO-15G, GO-20G, GO-30G, GO-40G, GO-60G, GO-XYZ SERIES, GO-DZ SERIES
FDA 510(k)
FDA Class 2
·Orthopedic
OT VERIO SYNC METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 8, 2014
STARCLOSE SE VASCULAR CLOSURE SYSTEM
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code MGB·June 6, 2013
LONG 45 ENDOCUTTER
FDA Adverse Event
Injury
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 6, 2011
TREVO XP PROVUE 4MM X 30MM
FDA Adverse Event
Injury
·STRYKER NEUROVASCULAR-UTAH-SALT LAKE CITY·Product code NRY·July 24, 2020