Home › Cordis US Corp. › Biopsy Forceps
Biopsy Forceps
Cordis US Corp. · Model 504300 · UDI-DI 10705032056090
DWZ
Prescription
1
510(k) clearances
89
Adverse events (1 deaths)
1
Recalls
24
Facilities
Description
BIOPSY FORCEPS 5.5F STD 104CM
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2005-04-12 | Heartport, Inc. | Guidewire is protruding through the film portion of the packages which compromises the sterility of the device. |
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.