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AESCULAP

Aesculap AG · Model DX509R · UDI-DI 04046963371531

EIF Prescription
4
510(k) clearances
15
Adverse events (1 deaths)
0
Recalls
169
Facilities

Description

Bone Split Retractor Storage, non-sterile, reusable

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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.