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AESCULAP

Aesculap AG · Model DP505R · UDI-DI 04038653038237

HXZ Prescription
1
510(k) clearances
513
Adverse events
1
Recalls
247
Facilities

Description

Wire Cutting Scissors, straight, 6 1/4", (160 mm), lateral cutting, hard wire up to Ø 1.2 mm, soft wire up to Ø 1.5 mm, non-sterilereusable

Recalls

DateFirmReason
2020-11-20Zimmer Biomet, Inc.Device has the potential for fracture during use.

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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.