13 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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TANITA BODY COMPOSITION ANALYZER, MODEL SC-331
FDA 510(k)
FDA Class 2
·Cardiovascular
BD 5ML SYRINGE LUER-LOK ¿ TIP
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMF·August 4, 2022
DATEX-OHMEDA S/5 NELLCOR COMPATIBLE SATURATION MODULE, M-NSAT AND ACCESSORIES
FDA 510(k)
FDA Class 2
·Cardiovascular
MULTITAK CONICAL TIP BONE SOFT TISSUE SUTURE ANCHOR
FDA 510(k)
FDA Class 2
·Orthopedic
BD LUER-LOK¿ SYRINGE BULK STERILE PHARMACY CONVENIENCE TRAY, 5 ML
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMF·June 30, 2022
NV GXL LINR, NTRL, 32MM ID, GROUP 2 CUPS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code MEH·July 20, 2022
NV GXL LNR, LIPPED, 36MM ID, GROUP 3 CUPS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JDI·July 9, 2024
CARPENTIER-EDWARDS PHYSIO ANNULOPLASTY RING
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code KRH·February 16, 2010
DISPOSABLE TECA CONCENTRIC NEEDLE
FDA Adverse Event
Injury
·NATUS MANUFACTURING LIMITED·Product code IKT·September 21, 2015
CONTOUR
FDA Adverse Event
Injury
·BAYER HEALTHCARE LLC·Product code NBW·May 2, 2013
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·September 15, 2014
NV GXL LINR, NTRL, 28MM ID, GROUP 1 CUPS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JDI·October 11, 2024
NV GXL LINR, NTRL, 36MM ID, GROUP 3 CUPS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JDI·October 28, 2024