14 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VIVIX-S 1751S
FDA 510(k)
FDA Class 2
·Radiology
Marina Medical
FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306822773·Shalita Expressor, 16cm
NO TRACE
FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807190611901·NO TRACE (TM) 018/LOWER 1,2 & 3 50T 0A
IN-OVATION® L
FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807190611001·IN-OVATION® L 018/LOWER 1&2 50T 0A
RS CARE LATEX MEDICAL EXAMINATION GLOVE (POWDER FREE)
FDA 510(k)
FDA Class 1
·General Hospital
REVOLUTION FULL CORE BIOPSY
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
VIDAS® CMV IGM
FDA Adverse Event
Malfunction
·BIOMERIEUX SA·Product code LKQ·March 11, 2019
ACCU-CHEK COMPACT TEST DRUM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·October 6, 2008
ACCU-CHEK SPIRIT COMBO
FDA Adverse Event
Malfunction
·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code LZG·July 27, 2011
SM PLUS BTT/ROUND BALLOON DISSECTOR
FDA Adverse Event
Malfunction
·COVIDIEN FORMERLY USSC PUERTO RICO·Product code GCJ·June 13, 2013
BD MAX¿ CPO
FDA Adverse Event
Malfunction
·GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)·Product code OOI·May 13, 2025
BD MAX¿ CPO
FDA Adverse Event
Malfunction
·GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)·Product code OOI·January 21, 2025
STEALTHSTATION¿ S8 SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC NAVIGATION, INC·Product code HAW·May 2, 2023
VENTED AUTOFEED HUMIDIFICATION CHAMBER
FDA Adverse Event
Malfunction
·Product code BTT·February 20, 2020