Home › Aesculap AG › A-SPACE SIBD
A-SPACE SIBD
Aesculap AG · Model ME613R · UDI-DI 04046963975531
HTR
Prescription
9
510(k) clearances
281
Adverse events (1 deaths)
2
Recalls
265
Facilities
Description
COBB A-SPACE SIBD Elevator, 30 °, angled, blunt, non-sterile, reusable
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2013-05-03 | Surgical Instrument Service And Savings, Inc. | The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch. |
| 2008-08-08 | Sterilmed Inc | SteriMed, Inc is conducting a product removal of a small group of devices individually packaged and sealed within a pouch. The removal is being conducted because the possibility e |
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.