33 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Integra Total Ankle Replacement System
FDA 510(k)
FDA Class 2
·Orthopedic
ProLift Trial
FDA UDI
Life Spine, Inc.·00190837087951·
HNM SPORTS MEDICINE
FDA UDI
HNM STAINLESS, LLC.·00842962101872·ETHOS PRO SMALL JOINT ANCHOR, PEEK, 2.9mm x 6mm...
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973837·
SYSMEX MODEL XE-2100DC AUTOMATED HEMATOLOGY ANALYZER
FDA 510(k)
FDA Class 2
·Hematology
OSTEORAPTOR II SUTURE ANCHOR OR TO BE DETERMINED MODEL: 72202764 72202765 72202766 72202767 72202768 72202769 72202770
FDA 510(k)
FDA Class 2
·Orthopedic
HNM SPORTS MEDICINE
FDA UDI
HNM STAINLESS, LLC.·00842962104088·ETHOS PRO SMALL JOINT ANCHOR, PEEK, 2.9mm x 6mm...
ROSA ONE
FDA Adverse Event
Injury
·MEDTECH SA·Product code HAW·November 10, 2017
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·April 11, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·March 15, 2018
ROSA ONE
FDA Adverse Event
Injury
·MEDTECH SA·Product code HAW·June 15, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·November 10, 2017
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·March 21, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·November 16, 2017
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·November 9, 2017
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·January 26, 2018
ROTORESTDELTA
FDA Adverse Event
Death
·ARJOHUNTLEIGH, INC.·Product code IKZ·October 6, 2014
ALTRUA
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·July 6, 2011
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·June 7, 2013
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·November 6, 2017