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Thoraflex™ Hybrid

VASCUTEK LTD · Model THA2426X150A · UDI-DI 05037881027005

QSK Prescription
0
510(k) clearances
323
Adverse events (34 deaths)
0
Recalls
4
Facilities

Description

Thoraflex Hybrid Ante-Flo Hybrid Stent Device

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.