Home › Aesculap AG › AESCULAP
AESCULAP
Aesculap AG · Model OG109R · UDI-DI 04046964072796
JYO
Prescription
7
510(k) clearances
7
Adverse events
1
Recalls
81
Facilities
Description
PLESTER Round Cutting Knife, straight, 6 1/4" (160 mm) (4,50 mm), width: 2,50 mm
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2013-03-27 | Summit Medical, Inc. | Summit Medical has initiated a recall of Myringotomy Lance Blade (Juvenile) because the box contains the wrong blade. The box contains Myringotomy Spear Blade (Juvenile). |
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.