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MAQUET SAS · Model ARD569069999 · UDI-DI 03700712400262

NTN FTD

510(k) clearances

273

Adverse events

Recalls

Facilities

Description

TUB 1100-60

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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.