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AESCULAP

Aesculap AG · Model DF352R · UDI-DI 04038653226221

JEP Prescription
3
510(k) clearances
15
Adverse events
0
Recalls
114
Facilities

Description

SET OF MATRIX RETAIN.NYSTROEM'S LE./RI.

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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.