60 results
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28ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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CALIBRATING MATERIAL, BUFFERS, STANDARD
FDA 510(k)
FDA Class 2
·Clinical Chemistry
OCTAGON BL NC Abutment 0° Ø 3.5 mm, L 5.5 mm GH 1.0 mm, cementable basic screw 2
FDA UDI
Hager & Meisinger Gesellschaft mit beschränkter Haftung·E0HM50220271·BL NC Abutment 0° Ø 3.5 mm, L 5.5 mm GH 1.0 mm,...
Safco polycarbonate crowns
FDA UDI
SAFCO DENTAL SUPPLY CO.·D72310220273·Safco polycar crwn ant/bicspd 120crwn
AOS CANCELLOUS SCREW 5.0mm x 27.5mm
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665019988·
MODIFICATION TO XIA SPINE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
FOCUS RADIATION TREATMENT PLANNING SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
BOSTON SCIENTIFIC BILIARY STENT
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code PNB·December 3, 2025
LOW SORBING SECONDARY SET SMARTSITE NEEDLE-FREE VALVE BAG ACCESS
FDA Adverse Event
Malfunction
·BD SWITZERLAND SARL·Product code LHI·March 25, 2026
LOW SORBING SECONDARY SET SMARTSITE NEEDLE-FREE VALVE BAG ACCESS
FDA Adverse Event
Malfunction
·BD SWITZERLAND SARL·Product code LHI·March 25, 2026
MARQUEE
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·August 9, 2024
PHASEAL CONNECTORS
FDA Adverse Event
Malfunction
·UNKNOWN·Product code ONB·May 7, 2026
DOSI FUSER ELASTOMERIC PUMP (250D2 TYPE); PHASEAL CONNECTORS
FDA Adverse Event
Malfunction
·EPIC INTERNATIONAL (THAILAND) CO., LTD.·Product code MEB·May 7, 2026
ROTAREX
FDA Adverse Event
Malfunction
·STRAUB MEDICAL AG·Product code MCW·August 28, 2024
PTFE FELT PLEDGETS
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code DXZ·March 2, 2023
OT VERIO IQ METER
FDA Adverse Event
Injury
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 26, 2013
SECURE II MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·March 10, 2011
DTC MARGRON HIP REPLACEMENT SYSTEM
FDA Adverse Event
Injury
·PORTLAND ORTHOPAEDICS LTD.·Product code LPH·April 1, 2008
25GX1IN HYPODERMIC NEEDLE-PRO EDGE SAFETY DEVICE
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC.·Product code FMI·June 15, 2023
PEN NEEDLE AUTOSHIELD DUO 30GX5MM EU
FDA Adverse Event
Malfunction
·EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND·Product code FMI·November 12, 2024
DENALI JUGULAR SYSTEM
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·July 30, 2024