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Lancing Device

Remote Patient Devices LLC · Model HH-XIII-T · UDI-DI 00860004687580

QRK
10
510(k) clearances
47
Adverse events
0
Recalls
82
Facilities

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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.