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Gimmi

Gimmi GmbH · Model KI.1506.18 · UDI-DI 04049047056591

HXZ Prescription
1
510(k) clearances
510
Adverse events
1
Recalls
246
Facilities

Description

STERNAL WIRE SEIZING FORCEPS TC, ROUND, 0.4 MM LENGTH 180 MM

Recalls

DateFirmReason
2020-11-20Zimmer Biomet, Inc.Device has the potential for fracture during use.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data 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.