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LAZIC
Peter Lazic GmbH · Model 74.355.00 · UDI-DI 04250603748595
KAE
Prescription
10
510(k) clearances
82
Adverse events
1
Recalls
225
Facilities
Description
Micro Cup Forceps straight, jaw: 1,8 x 0,6 x 4,5 mm shaft length 180 mm / 7"
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-01-31 | Aesculap Inc | The forceps have been used in ways not covered by the design resulting in breakage of the clamps. |
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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.
