10 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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MODIFICATION TO MP-3 POWER BASE CHAIR
FDA 510(k)
FDA Class 2
·Physical Medicine
artegral life
FDA UDI
Merz Dental GmbH·D7091993032·anteriors; shade A1; mould UBIS
GALAXY FIXATION SYSTEM
FDA UDI
ORTHOFIX SRL·18054242518969·GALAXY TL-HEX CONNECTING POST L100MM D12MM STERILE
KY Grosz Liquid
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
TRIAGE TOTAL 3 CONTROLS AND CALIBRATION VERIFICATION SET
FDA 510(k)
FDA Class 1
·Clinical Chemistry
SPECIFIC DEVICE NOT REPORTED
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JDI·June 18, 2024
DIMENSION VISTA® CLINICAL CHEMISTRY SYSTEM
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS INC - GLASGOW·Product code MMI·March 7, 2013
PARADIGM INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code LZG·February 7, 2011
CAPSUREFIX MRI SURESCAN
FDA Adverse Event
Injury
·MPRI·Product code NVN·August 8, 2014
WALLSTENT? RP ENDOPROSTHESIS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·July 21, 2025