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KENEX

KENEX (ELECTRO-MEDICAL) LIMITED · Model 1501/D · UDI-DI 05055449416009

FRK Prescription
4
510(k) clearances
652
Adverse events (1 deaths)
1
Recalls
69
Facilities

Description

Hydraulic Patients Chair

Recalls

DateFirmReason
2021-05-12Stryker Medical Division of Stryker CorporationMedical devices intended for use in a healthcare facility were distributed to residential customers and may be in use in a home environment. The product s labeling accurately iden

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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.