Home › KENEX (ELECTRO-MEDICAL) LIMITED › KENEX
KENEX
KENEX (ELECTRO-MEDICAL) LIMITED · Model 354/P76/LED150F-0031 · UDI-DI 05055449409902
EAK
Prescription
7
510(k) clearances
10
Adverse events
0
Recalls
21
Facilities
Description
354/P76/LED150F-0031 76x61cm Shield withArm,Column,LED150F Lmp & Alu Track
Query this across every FDA database — by API.
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.
