Data / Medical devices / Ventilatory Effort Recorder / United Kingdom
FDA-registered makers of Ventilatory Effort Recorder in the United Kingdom: 5 establishments
5 establishments in the United Kingdom are registered with the FDA to make Ventilatory Effort Recorder (product code MNR). 1 has a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Ventilatory Effort Recorder
- Product code
- MNR
- Country
- United Kingdom
Makers of Ventilatory Effort Recorder in the United Kingdom
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Acurable Limited | London, United Kingdom | Exporter to the US, Specification developer | 2 | February 3, 2023 | 0 | 0 | 0 | api.fda.gov |
| Cogent Technology Limited | Felixstowe Suffolk, United Kingdom | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| GVS Filter Technology UK Ltd | Lancaster Lancashire, United Kingdom | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Remote Diagnostic Technologies Ltd. | FARNBOROUGH Hampshire, United Kingdom | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Spacelabs Healthcare Ltd. | HERTFORD Hertfordshire, United Kingdom | Specification developer | 0 | 0 | 1 | 0 | api.fda.gov |
Updated November 2, 2026. 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.