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AESCULAP
AESCULAP, INC. · Model MA255R · UDI-DI 04046964585845
KAD
Prescription
5
510(k) clearances
21
Adverse events
1
Recalls
120
Facilities
Description
GUILFORD-WRIGHT Elevator, 5 1/2", (140 mm), width: 2 mm, non-sterile, reusable
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-12-03 | Sklar Instruments | Reports of various packaging issues that may result in a breach of the sterile barrier. |
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Get your free API keyRead the docsData 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.