Data / Medical devices / Stretcher, Patient Restraint

Stretcher, Patient Restraint (NZD): 51 FDA-registered makers in 14 countries

51 establishments in 14 countries are registered with the FDA to make Stretcher, Patient Restraint (product code NZD, Class 1, 21 CFR 880.6900). 0 of them have a 510(k) clearance or PMA approval on file and 1 has a recall event. The FDA has issued 1 510(k) clearance under this code, the latest on August 17, 2006, and lists 1 recall event (0 Class I). FDA data exported November 2, 2026.

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Product code

NZD

Device class

1

Regulation

880.6900

Medical specialty

General Hospital

Makers by country

Makers of Stretcher, Patient Restraint

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 August 17, 2006. 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.