25 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Neuro Omega System
FDA 510(k)
FDA Class 2
·Neurology
Brasseler
FDA UDI
Provision·B504OMKM715810·
NA
FDA UDI
STERILMED, INC.·10888551007689·SAW BLADE OSCILLATING LARGE BONE
BACKPACK MEDICAL OXYGEN SYSTEM
FDA 510(k)
FDA Class 2
·Anesthesiology
INTUITIVE SURGICAL DA VINCI S SURGICAL SYSTEM WITH DA VINCI CONNECT & DA VINCI ONSITE, MODEL IS2000
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
JAMSHIDI BONE MARROW TRAY 11G X4 15G ASP
FDA Adverse Event
Malfunction
·CAREFUSION, INC·Product code KNW·March 12, 2026
AU680 CLINICAL CHEMISTRY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code JJE·October 14, 2014
SCRDRIVER F/EXTRACT
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code HXX·June 15, 2013
INSIGNIA
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·July 21, 2011
BD INTIMA-II Y 24GAX0.75IN PRN EC SLM NPVC
FDA Adverse Event
Malfunction
·BD (SUZHOU)·Product code FOZ·January 2, 2024
BD INTIMA-II Y 24GAX0.75IN PRN EC SLM NPVC
FDA Adverse Event
Malfunction
·BD SUZHOU (MDS)·Product code FOZ·March 13, 2024
BD INTIMA-II Y 24GAX0.75IN PRN EC SLM NPVC
FDA Adverse Event
Malfunction
·BD (SUZHOU)·Product code FOZ·December 21, 2023
BD INTIMA-II Y 24GAX0.75IN PRN EC SLM NPVC
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FOZ·December 18, 2024
ALINITY S HTLV I/II REAGENT KIT
FDA Adverse Event
Injury
·ABBOTT GMBH·Product code QHM·September 29, 2022
ALINITY S HTLV I/II REAGENT KIT
FDA Adverse Event
Injury
·ABBOTT GMBH·Product code QHM·September 29, 2022
ALINITY S HTLV I/II REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code QHM·September 29, 2022
ALINITY S HTLV I/II REAGENT KIT
FDA Adverse Event
Injury
·ABBOTT GMBH·Product code QHM·September 29, 2022
ALINITY S HTLV I/II REAGENT KIT
FDA Adverse Event
Injury
·ABBOTT GMBH·Product code QHM·September 29, 2022
ALINITY S HTLV I/II REAGENT KIT
FDA Adverse Event
Injury
·ABBOTT GMBH·Product code QHM·September 29, 2022
JAMSHIDI BONE MARROW TRAY 11G X4 15G ASP
FDA Adverse Event
Malfunction
·CAREFUSION, INC·Product code LWE·October 8, 2025