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SUGITA ANEURYSM CLIP
MIZUHO CORPORATION · Model 07-940-32 · UDI-DI 04946329060973
HCI
Prescription
10
510(k) clearances
54
Adverse events
5
Recalls
10
Facilities
Description
TYPE: FENESTRATED LARGE, PERMANENT, No.32 RANGE: 95-135gf(0.93-1.32N) MATERIAL: ISO 5832-7/ASTM F1058G2 BLADE: BENT MAXIMUM OPENING: 8.0mm GRIP SURFACE: SERRATED
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-10-06 | Peter Lazic Gmbh | Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip. |
| 2023-10-06 | Peter Lazic Gmbh | Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip. |
| 2023-10-06 | Peter Lazic Gmbh | Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip. |
| 2007-11-01 | Aesculap Inc | Breakage: the inner rod of the applier may corrode and break |
| 2007-11-01 | Aesculap Inc | Breakage: the inner rod of the applier may corrode and break |
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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.