5,532 results · 35ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

Protem Fixture Driver Assy

FDA UDI
DIO Corporation·08800049200728·

Protem Fixture Driver Assy

FDA UDI
DIO Corporation·08800049200643·

Protem Fixture Driver Assy

FDA UDI
DIO Corporation·08800049200698·

Protem Fixture Driver Assy

FDA UDI
DIO Corporation·08800049200629·

Protem Fixture Driver Assy

FDA UDI
DIO Corporation·08800049200636·

Protem Fixture Driver Assy

FDA UDI
DIO Corporation·08800049200667·

Protem Fixture Driver Assy

FDA UDI
DIO Corporation·08800049200735·

Protem Fixture Driver Assy

FDA UDI
DIO Corporation·08800049200674·

Protem Fixture Driver Assy

FDA UDI
DIO Corporation·08800049200711·

Protem Fixture Driver Assy

FDA UDI
DIO Corporation·08800049200681·

Protem Fixture Driver Assy

FDA UDI
DIO Corporation·08800049200704·

Protem Fixture Driver Assy

FDA UDI
DIO Corporation·08800049200650·

LIBERTY CYCLER SET, SINGLE CONN./EXT. DL

FDA Adverse Event
Malfunction ·REYNOSA MGR·Product code FKX·February 25, 2015

Rexton

FDA UDI
Ws Audiology Usa, Inc.·04056839107089·Rexton HA ADORE M GR Hearing Aid

ABBOTT PAIN MGR

FDA Adverse Event
Death ·ABBOTT LABORATORIES·Product code MEA·December 18, 2003

ABBOTT PAIN MGR

FDA Adverse Event
Injury ·HOSPIRA, INC.·Product code FRN·December 13, 2004

TRIUMPH-1 PORT

FDA Adverse Event
Malfunction ·HORIZON MEDICAL PRODUCTS, INC.·Product code LJT·April 27, 2000

ABBOTT PAIN MGR II

FDA Adverse Event
Malfunction ·ABBOTT LABORATORIES·Product code FPA·August 15, 2003

ABBOTT PAIN MGR II

FDA Adverse Event
Malfunction ·ABBOTT LABORATORIES·Product code MEA·August 15, 2003

ABBOTT PAIN MGR II

FDA Adverse Event
Malfunction ·ABBOTT LABORATORIES·Product code MEA·August 15, 2003