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Aqua Liner L

Romedis GmbH · Model SA701.4L · UDI-DI 04260652350045

ISS
1
510(k) clearances
29
Adverse events
0
Recalls
46
Facilities

Description

Liner to be worn over residual limb

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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.