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AESCULAP

Aesculap AG · Model FO930R · UDI-DI 04038653169719

HRT Prescription
0
510(k) clearances
21
Adverse events
0
Recalls
102
Facilities

Description

REILL Tendon Stripper, 15 3/4" (400 mm), diam. 6 mm, closed, shaft length: 350 mm

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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.