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HEP

Heidelberg Engineering GmbH · Model HEP with HEYEX 2 SW V3.2c · UDI-DI 04059237000372

HOO Prescription
6
510(k) clearances
0
Adverse events
0
Recalls
12
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.