10,000 results
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59ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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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