23 results · 27ms · Sources: EU EUDAMED, US FDA

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K181166

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code CBK·December 2, 2022

TRILOGY EVO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code CBK·July 15, 2020

Trilogy Evo

FDA 510(k)
FDA Class 2 ·Anesthesiology

TRILOGY EVO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC·Product code CBK·August 17, 2020

TRILOGY EVO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code CBK·May 21, 2020

TRILOGY EVO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC·Product code CBK·August 12, 2020

TRILOGY EVO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC·Product code CBK·July 8, 2020

TRILOGY EVO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC·Product code CBK·July 8, 2020

TRILOGY EVO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC·Product code CBK·June 26, 2020

TRILOGY EVO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC·Product code CBK·July 8, 2020

TRILOGY EVO, O2, BRAZIL

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code CBK·September 6, 2024

TRILOGY EVO, BRAZIL

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code CBK·September 6, 2024

TRILOGY EVO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC·Product code CBK·August 19, 2020

TRILOGY EVO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC·Product code CBK·July 24, 2020

TRILOGY 100

FDA Adverse Event
Malfunction ·RESPIRONICS, INC·Product code CBK·July 7, 2020

LIFEVENT EVO2

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code CBK·May 27, 2025

PILLING

FDA UDI
TELEFLEX INCORPORATED·24026704512571·

LIGHTSTREAM LOW LEVEL LASER

FDA 510(k)
FDA Class 2 ·Physical Medicine

4D-VIEW 9.1 (4D VIEW PC SOFTWARE) MODEL: H48651SZ

FDA 510(k)
FDA Class 2 ·Radiology

MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM

FDA Adverse Event
Malfunction ·MED-EL ELEKTROMEDIZINISCHE GERAETE, GMBH·Product code MCM·July 8, 2011