16 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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aprevo® TLIF-C Articulating System
FDA 510(k)
FDA Class 2
·Orthopedic
Mui Scientific
FDA UDI
H & A Mui Enterprises Inc·10678467505207·Customized Single-Use HRM, Esophageal 24-ch Cat...
Mui Scientific
FDA UDI
H & A Mui Enterprises Inc·00678467006592·Customized Reusable Aspiration 24 Channel Catheter
Mui Scientific
FDA UDI
H & A Mui Enterprises Inc·00678467006257·Customized Reusable Anorectal 24 Channel Cathet...
Mui Scientific
FDA UDI
H & A Mui Enterprises Inc·10678467505382·24-Channel Customized Single-Use Anorectal Cath...
Portex
FDA UDI
ICU MEDICAL, INC.·15019517071368·
AMICUS SEPARATOR SYSTEM/ AMICUS SEPERATOR SYSTEM;REFURBISHED
FDA 510(k)
FDA Unclassified
·Unknown
THE FUGO BLADE FOR GLAUCOMA
FDA 510(k)
FDA Class 2
·Ophthalmic
UNKNOWN LIGASURE INSTRUMENT
FDA Adverse Event
Injury
·US SURGICAL PUERTO RICO·Product code GEI·January 18, 2021
UNKNOWN ENDO GIA SULU
FDA Adverse Event
Injury
·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·January 18, 2021
UNKNOWN TA
FDA Adverse Event
Injury
·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·January 18, 2021
12/14 ARTICUL 40MM M SPEC +12
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code LPH·November 19, 2008
TERUMO CDI 5000 BLOOD PARAMETER MONITOR
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEM CORP.·Product code DRY·August 17, 2011
FLEXCATH STEERABLE SHEATH
FDA Adverse Event
Malfunction
·MEDTRONIC CRYOCATH LP·Product code DRA·July 22, 2013
UNKNOWN CUSA EXCEL
FDA Adverse Event
Injury
·INTEGRA LIFESCIENCES(IRELAND)·Product code LFL·June 3, 2019
UNKNOWN CUSA EXCEL
FDA Adverse Event
Injury
·INTEGRA LIFESCIENCES(IRELAND)·Product code LFL·June 3, 2019