42 results · 33ms · Sources: EU EUDAMED, US FDA

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EnSite X EP System, Advisor VL Circular Mapping Catheter, Sensor Enabled, Advisor FL Circular Mapping Catheter, Sensor Enabled, Advisor HD Grid High Density Mapping Catheter, Senor Enabled

FDA 510(k)
FDA Class 2 ·Cardiovascular

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112496·BARRON VACUUM TREPHINE 7.5MM

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112533·BARRON VACUUM TREPHINE 8.5MM

SprintRay High Impact Denture Teeth - A1

FDA UDI
Sprintray, Inc.·00850039704307·SprintRay High Impact Denture Teeth is a light-...

FREEZER TEETHER

FDA 510(k)
FDA Class 2 ·Dental

REGISTRADO X-TRA

FDA 510(k)
FDA Class 2 ·Dental

Trabecular Metal®

FDA UDI
Zimmer, Inc.·00889024119079·

Trabecular Metal®

FDA UDI
Zimmer, Inc.·00889024119086·

Trabecular Metal®

FDA UDI
Zimmer, Inc.·00889024119093·

UNKNOWN LIGASURE INSTRUMENT

FDA Adverse Event
Injury ·COVIDIEN MFG DC BOULDER·Product code GEI·October 21, 2020

ENDURANT STENT GRAFT

FDA Adverse Event
Malfunction ·MEDTRONIC IRELAND·Product code MIH·September 29, 2020

TALENT AAA STENT GRAFT

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code MIH·September 29, 2020

TALENT AAA STENT GRAFT

FDA Adverse Event
Malfunction ·MEDTRONIC IRELAND·Product code MIH·September 29, 2020

ENDURANT STENT GRAFT

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code MIH·September 29, 2020

ENDURANT STENT GRAFT

FDA Adverse Event
Malfunction ·MEDTRONIC IRELAND·Product code MIH·September 29, 2020

ENDURANT STENT GRAFT

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code MIH·September 29, 2020

OXIMAX N-595 PULSE OXIMETER

FDA Adverse Event
Malfunction ·COVIDIEN FORMERLY TYCO HEALTHCARE·Product code DQA·October 15, 2008

HEARTMATE II LVAS

FDA Adverse Event
Injury ·THORATEC CORP.·Product code DSQ·June 27, 2013

ANEURX AAADVANTAGE STENT GRAFT SYSTEM - HYDRO

FDA Adverse Event
Injury ·MEDTRONIC CARDIOVASCULAR·Product code MIH·August 5, 2011

Barron Radial Vacuum Trephine (1) Complete Trephine Set 9.0mm Dia. Ref. K20-2062 Lot 122336 Opthalmic

FDA Recall
Terminated ·Surgical Instrument Service And Savings, Inc.·Product code HRH·May 3, 2013