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AESCULAP

Aesculap AG · Model DB629R · UDI-DI 04038653147229

EMN Prescription

510(k) clearances

Adverse events

Recalls

223

Facilities

Description

INSERTER TO CHANGE WORKING TIPS

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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.