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MicroFrance®

INTEGRA MICROFRANCE · Model 7783-12 · UDI-DI 10381780089209

KCP Prescription
4
510(k) clearances
26
Adverse events
1
Recalls
143
Facilities

Description

MicroFrance® Chouard pushing syringe for disposable syringe luer-lock

Recalls

DateFirmReason
2003-04-30Medegen Medical Products, LLCFinished products were not sterilized.

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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.