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Medi-First Latex Medium Finger Cots

Medique Products · Model 70435 · UDI-DI 00347682704353

LZB
5
510(k) clearances
1
Adverse events
1
Recalls
71
Facilities

Description

A non-powdered patient disposable latex device intended for medical purposes that is worn on the examiner's finger to prevent contamination between patient and examiner. (144 count)

Recalls

DateFirmReason
2016-03-31American Surgical CompanyProduct packaging defective compromising sterility

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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.