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HI-LINE

Aesculap AG · Model GD710R · UDI-DI 04038653300570

GEF Prescription
4
510(k) clearances
580
Adverse events
0
Recalls
29
Facilities

Description

HI-LINE DIAMOND BURR II EXCEPT.LG.D3.1MM

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.