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ActivL

Highridge Medical, LLC · Model BT070R-HM · UDI-DI 03662663083560

KIK Prescription
1
510(k) clearances
17
Adverse events
0
Recalls
114
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.