30 results · 39ms · Sources: EU EUDAMED, US FDA

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CELOX TRAUMA GAUZE AG, CELOX HEMOSTATIC ANTIBACTERIAL TRAUMA GAUZE, OMNI-STAT TRAUMA GAUZE AG, OMNI-STAT HEMOSTATIC ANTI

FDA 510(k)
FDA Unclassified ·Unknown

Recon

FDA UDI
Revelation Medical Devices·G3181029650·Taylor Retractor

STERILE SALINE SOLUTION

FDA 510(k)
FDA Class 2 ·Ophthalmic

SONOACE R7 DIAGNOSTIC ULTRASOUND SYSTEM

FDA 510(k)
FDA Class 2 ·Radiology

BIPAP A30

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNS·March 31, 2022

BIPAP ST

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

BIPAP ST

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

BIPAP AVAPS

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

BIPAP ST

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNS·March 3, 2022

BIPAP A30

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

BIPAP AVAPS

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

BIPAP ST

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

BIPAP A30

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNS·March 30, 2022

BIPAP AVAPS

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNS·March 16, 2022

BIPAP AVAPS

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

BIPAP ST

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

ELECTRIC PEN DRIVE 60,000 RPM

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code HWE·May 9, 2013

MECHANICAL WALKER, ROLLATOR

FDA Adverse Event
KENSTONE METAL·Product code ITJ·September 19, 2014

RUSCH GOLD 2-WAY SILICONE FOLEY, 16FR

FDA Adverse Event
Malfunction ·TELEFLEX MEDICAL·Product code EZL·May 11, 2011

BD INSYTE AUTOG BC

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·November 12, 2024