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AESCULAP
Aesculap AG · Model DF250R · UDI-DI 04038653242849
EKH
Prescription
3
510(k) clearances
17
Adverse events (1 deaths)
1
Recalls
96
Facilities
Description
WESTCOTT Carving Instrument, 7" (175 mm), double ended, ergonomic handle, peek handle, Fig. 21, green
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-04-20 | Almore International Inc | Microfil Composite Instruments were distributed with a sterile symbol on their packaging label inserts, indicating that the products are sold as sterile devices. These products are |
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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.