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Amoena

AMOENA Medizin-Orthopädie-Technik GmbH · Model 010 Strips (04) · UDI-DI 04026275447476

MDA Prescription
10
510(k) clearances
51
Adverse events (1 deaths)
0
Recalls
190
Facilities

Description

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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.