11 results
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19ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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CHLORINATED, POLYMER COATED, POWDER-FREE LATEX EXAMINATION GLOVE
FDA 510(k)
FDA Class 1
·General Hospital
PE/Cyanine7 anti-human CD13
FDA UDI
BIOLEGEND, INC.·00810034701640·URL: https://www.biolegend.com/en-us/products/p...
MEDIUM 199, CATALOG NO. 200-2032
FDA 510(k)
FDA Class 1
·Hematology
SPINNING SPIROS, MODEL CH-2000
FDA 510(k)
FDA Class 2
·General Hospital
SPINNING SPIROS® CLOSED MALE LUER, RED CAP
FDA Adverse Event
Malfunction
·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code FPA·November 4, 2025
CADD LEGACY PLUS PUMP
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC.·Product code FRN·January 20, 2025
SMART PERFUSION PACK: APEX MBR FMC/MID WEST REG LEXINGTON, KY
FDA Adverse Event
Injury
·Product code DTZ·September 11, 2007
CADD LEGACY PLUS PUMP
FDA Adverse Event
Malfunction
·ST PAUL·Product code FRN·September 9, 2022
NAVILYST MEDICAL
FDA Adverse Event
Malfunction
·NAVILYST MEDICAL·Product code LJS·June 13, 2014
INTERFACE 8252800 RESPONSE 2.0 INCREMENT
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED, INC.·Product code ETN·February 25, 2013
ACCU-CHEK ® AVIVA TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·February 9, 2011