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MIV

FDA UDI
Merit Medical·00884450281277·

ABC Nipple

FDA UDI
AMERICAN BREAST CARE, L.P.·00811749024765·Nipple prosthesis, external 906 ABC Nipple Made...

THE SIGNATURE SERIES, M IV

FDA 510(k)
FDA Class 2 ·Neurology

MODIFIED M-IV MAMMOGRAPHY SYSTEM

FDA 510(k)
FDA Class 2 ·Radiology

Merit SwiftNINJA®

FDA UDI
Merit Medical Systems, Inc.·00884450324004·

Merit SwiftNINJA®

FDA UDI
Merit Medical Systems, Inc.·00884450278505·

MCC-MIV ONE 2 ONE SOFTWARE

FDA 510(k)
FDA Class 2 ·Physical Medicine

LORAD M-IV, LORAD M-IVI

FDA 510(k)
FDA Class 2 ·Radiology

LORAD MIV MAMMOGRAPHY SYSTEM

FDA Adverse Event
Injury ·HOLOGIC, INC.·Product code IZH·September 22, 2009

EUROCART SR-4, EUROCART M-IV, ISOCART III

FDA 510(k)
FDA Class 1 ·Dental

LORAD MIV MAMMAGRAPHY SYSTEMS

FDA Adverse Event
Other ·HOLOGIC, INC.·Product code IZH·April 19, 2005

CTR73, 12X100 KII OPT ZTHR 6/BX

FDA Adverse Event
Malfunction ·APPLIED MEDICAL RESOURCES·Product code GCJ·December 16, 2022

TRIFURCATED EXTENSION SET

FDA Adverse Event
Malfunction ·VYGON USA·Product code FPA·May 10, 2022

MIV MAMMOGRAPHY SYSTEM

FDA Adverse Event
HOLOGIC, INC.·Product code IZH·June 29, 2016

UNSPECIFIED BD PRI TUBING

FDA Adverse Event
Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.·Product code LHI·July 20, 2020

XPANDER, 15/3 IBT

FDA Adverse Event
Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code HRX·September 19, 2013

XPANDER, 15/3 IBT

FDA Adverse Event
Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code HRX·September 19, 2013

XPANDER, 15/3 IBT

FDA Adverse Event
Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code HRX·September 19, 2013

XPANDER, 15/3 IBT

FDA Adverse Event
Malfunction ·KYPHON NEUCHATEL·Product code HRX·September 19, 2013

SELENIA MAMMOGRAPHY SYSTEM

FDA Adverse Event
Malfunction ·HOLOGIC, INC.·Product code MUE·January 5, 2018