Home › Aesculap AG › AESCULAP
AESCULAP
Aesculap AG · Model OM090R · UDI-DI 04038653179077
KAI
Prescription
9
510(k) clearances
4
Adverse events
1
Recalls
109
Facilities
Description
Laryngeal Mirror, 7" (180 mm), diam. 30 mm, hexagonal handle, Fig. 10
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-02-23 | MEDLINE INDUSTRIES, LP - Northfield | Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.