Data / Medical devices / Monitor, Bed Patient

Monitor, Bed Patient (KMI): 86 FDA-registered makers in 11 countries

86 establishments in 11 countries are registered with the FDA to make Monitor, Bed Patient (product code KMI, Class 1, 21 CFR 880.2400). 1 of them has a 510(k) clearance or PMA approval on file and 5 have a recall event. The FDA has issued 31 510(k) clearances under this code, the latest on November 10, 2014, and lists 16 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code

KMI

Device class

1

Regulation

880.2400

Medical specialty

General Hospital

Makers by country

Makers of Monitor, Bed Patient

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

Updated November 10, 2014. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.