156 results
·
50ms
·
Sources: EU EUDAMED, US FDA
FasTouch™ Absorbable
FDA UDI
VIA SURGICAL LTD·07290017155241·Sample of the FasTouch™ Absorbable Fixation Sys...
TissueTak™
FDA UDI
VIA SURGICAL LTD·07290017155302·TissueTak™ Absorbable Fixation System
10 Absorb...
FasTouch™ Absorbable
FDA UDI
VIA SURGICAL LTD·07290017155289·Sample of the FasTouch™ Absorbable Reloadable C...
TissueTak™
FDA UDI
VIA SURGICAL LTD·07290017155364·TissueTak™ Absorbable Fixation System 10 Absorb...
TissueTak™
FDA UDI
VIA SURGICAL LTD·07290017155357·Non-Sterile Sample of the TissueTak™ Permanent ...
TissueTak™
FDA UDI
VIA SURGICAL LTD·07290017155340·Non-Sterile Sample of the TissueTak™ Absorbable...
FasTouch™ Absorbable
FDA UDI
VIA SURGICAL LTD·07290017155210·FasTouch™ Absorbable Fixation System - 25 Absor...
FasTouch™
FDA UDI
VIA SURGICAL LTD·07290017155012·Sterile Sample of the FasTouch™ Permanent Fixat...
FasTouch™
FDA UDI
VIA SURGICAL LTD·07290017155104·FasTouch™ Permanent Fixation System
25 Permanen...
FasTouch™
FDA UDI
VIA SURGICAL LTD·07290017155111·FasTouch™ Permanent Reloadable Cartridge
10 Per...
FasTouch™ Absorbable
FDA UDI
VIA SURGICAL LTD·07290017155272·FasTouch™ Absorbable Reloadable Cartridge - 10 ...
FasTouch™
FDA UDI
VIA SURGICAL LTD·07290017155043·Sterile Sample of the FasTouch™ Permanent Reloa...
FASTOUCH ABSORBABLE 5MM FIXATION SYSTEM
FDA Adverse Event
Injury
·VIA SURGICAL LTD.·Product code GDW·April 13, 2021
CELT ACD VASCULAR CLOSURE DEVICE
FDA Adverse Event
Injury
·VASORUM LTD.·Product code MGB·June 17, 2024
OUTBACK RE-ENTRY CATHETER
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code DQY·March 4, 2014
CORDIS LUMEND OUTBACK LTD RE-ENTRY CATHETER
FDA Adverse Event
Other
·Product code DQY·October 7, 2008
LUMEND OUTBACK LTD RE-ENTRY CATHETER
FDA Adverse Event
Other
·CORDIS·Product code DQY·September 9, 2008
GELWEAVE
FDA Adverse Event
Injury
·VASCUTEK LTD·Product code DSY·November 3, 2021
COMPRESSION ANASTOMOSIS RING CAR 27/COLONRING
FDA Adverse Event
Injury
·NITI SURGICAL SOLUTIONS LTD.·Product code FZP·August 23, 2010
CORDIS LUMEND OUTBACK LTD RE-ENTRY CATHETER
FDA Adverse Event
CORDIS·Product code DQY·August 28, 2008