10 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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Hill-Rom Wireless Connectivity Module
FDA 510(k)
FDA Class 2
·Physical Medicine
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526550193·GENUMEDI PT KNEE SUP SILVER R EW IV
HNM MEDICAL
FDA UDI
HNM STAINLESS, LLC.·00842962113554·METZENBAUM SCISSORS, 5 1/2", STR, SUPERCUT
VENUS CERVICAL SPINAL FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
HL 188 & HL 189 BODY FAT METER
FDA 510(k)
FDA Class 2
·Cardiovascular
POWERHEART G5 AUTOMATIC AED
FDA Adverse Event
Malfunction
·CARDIAC SCIENCE CORPORATION·Product code MKJ·October 18, 2018
LOANER CORE UNIVERSAL DRIVER
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS-KALAMAZOO·Product code ERL·October 6, 2014
UPHOLD VAGINAL SUPPORT SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 3, 2013
SPEEDICATH CH10 MALE
FDA Adverse Event
Malfunction
·COLOPLAST A/S·Product code GBM·June 29, 2011
Medtronic MiniMed(TM) Mio(TM) (MMT-921, 921T, 923, 923T, 925, 925T, 941, 941T, 943, 943T, 945, 945T, 961, 963, 963T, 965, 965T, 975, 975T)
FDA Enforcement
Class II
·Ongoing·Medtronic Inc.·November 29, 2017