156 results · 50ms · Sources: EU EUDAMED, US FDA

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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