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AESCULAP

Aesculap AG · Model DL363R · UDI-DI 04038653036981

EMJ Prescription
6
510(k) clearances
641
Adverse events
0
Recalls
237
Facilities

Description

Root Elevator, straight, 6", (150 mm), handle with thumb depression, Fig. 3S, width: 3,500 mm, non-sterile, reusable

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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.