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KENEX

KENEX (ELECTRO-MEDICAL) LIMITED · Model 351/P/LR · UDI-DI 05055449401791

EAK Prescription
7
510(k) clearances
10
Adverse events
0
Recalls
22
Facilities

Description

Curtain fitted to 80cm wide shield - with cut-ouT

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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.