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Highlander

Harmar Summit, LLC · Model Highlander II · UDI-DI 00817650023972

PCE
1
510(k) clearances
12
Adverse events (1 deaths)
0
Recalls
12
Facilities

Description

Platform lift, 14 ft, Standard, commercial, hoistway, battery, indoor

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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.