Home › Aesculap AG › AESCULAP
AESCULAP
Aesculap AG · Model GC681R · UDI-DI 04046963839345
DWH
Prescription
4
510(k) clearances
159
Adverse events (1 deaths)
1
Recalls
35
Facilities
Description
STERNUM SAW BL.RAPID ACT.35/75/0.7/0.9MM
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2011-11-17 | Terumo Cardiovascular Systems Corporation | Terumo Cardiovascular Systems has received one report of minute metal shavings leaking from the Sarns Sternal Saw I System at the point where the saw blade is inserted into the saw |
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.