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Sleeve heavy-duty1

Romedis GmbH · Model SA900 · UDI-DI 04260652350106

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

Description

sleeve worn over residual limb/socket

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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.