Home › Aesculap AG › AESCULAP
AESCULAP
Aesculap AG · Model FX006SU · UDI-DI 04041906505585
GYK
Prescription
10
510(k) clearances
15
Adverse events
1
Recalls
21
Facilities
Description
TUNNELLER 450MM STANDARD
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2010-12-22 | Integra LifeSciences Corp. | Peritoneal Introducer Sheaths were incorrectly labeled as 61 cm instead of 46 cm. |
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.