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AESCULAP
AESCULAP, INC. · Model MG010R · UDI-DI 04046964573835
DWP
Prescription
10
510(k) clearances
171
Adverse events
1
Recalls
44
Facilities
Description
DE BAKEY Vascular Dilator, 7 1/2", (190 mm), diam. 10 mm, non-sterile, reusable
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-12-06 | Baxter Healthcare Corporation | Cardiovascular Surgery marketing brochure (US-AS46-220001) that was distributed for the products listed below contains inaccurate content that does not align with some of the produ |
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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.