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AESCULAP
AESCULAP, INC. · Model EF803R · UDI-DI 04046964580710
FBX
Prescription
1
510(k) clearances
16
Adverse events
1
Recalls
54
Facilities
Description
VAN BUREN Urethral Catheter, 10 5/8" (270 mm), 14FR
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.