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AESCULAP
Aesculap AG · Model EA880R · UDI-DI 04038653221868
FER
Prescription
10
510(k) clearances
86
Adverse events
1
Recalls
47
Facilities
Description
IVES-FANSLER ANUSCOPE 24X78MM
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-12-12 | Applied Medical Resources Corp | Unintentional shifting of the tip insulation of the firm's electrosurgical probes. |
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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.