20 results · 25ms · 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.

Aneroid sphygmomanometer with stethoscope, Aneroid sphygmomanometer

FDA 510(k)
FDA Class 2 ·Cardiovascular

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172970584·

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172970126·

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172970591·

ARP RX100

FDA 510(k)
FDA Class 2 ·Physical Medicine

NOTOUCH BREASTSCAN

FDA 510(k)
FDA Class 1 ·Obstetrics/Gynecology

NEXTAR INFRARED CAMERA

FDA Adverse Event
Malfunction ·MEDACTA INTERNATIONAL SA·Product code JWH·September 10, 2021

OMNIPOD 5 POD

FDA Adverse Event
Malfunction ·INSULET CORPORATION·Product code QFG·February 13, 2023

OMNIPOD 5 POD

FDA Adverse Event
Malfunction ·INSULET CORPORATION·Product code QFG·February 13, 2023

OMNIPOD 5 POD

FDA Adverse Event
Malfunction ·INSULET CORPORATION·Product code QFG·February 13, 2023

SEGURA HEMISPHERE STONE RETRIEVAL BASKET

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC·Product code FFL·October 7, 2008

MICRO-MATE TURBERCULIN GLASS SYRINGE

FDA Adverse Event
Malfunction ·CADENCE INC.·Product code DWO·June 25, 2013

HIP DRILLS & GUIDES

FDA Adverse Event
Malfunction ·SMITH & NEPHEW ENDOSCOPY·Product code NBH·August 5, 2011

DURAL ALPHA INSERT W RIM II/32

FDA Adverse Event
Malfunction ·ZIMMER GMBH·Product code LPH·March 12, 2019

DURASUL, ALPHA INSERT, HOODED, II/32

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code LPH·September 28, 2018

METASUL, ALPHA INSERT, JJ/28

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code KWA·February 4, 2019

DURASUL, ALPHA INSERT, KK/36

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code JDI·March 13, 2018

COCR HEAD 32/ 0 'M' 12/14

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code JDI·June 4, 2019

DURASUL, ALPHA INSERT, LL/36

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code JDI·April 29, 2019

DURASUL, ALPHA INSERT, HOODED, KK/32

FDA Adverse Event
Malfunction ·ZIMMER GMBH·Product code LPH·June 15, 2018