Data / Medical devices / United Kingdom / BPR Medical Limited
BPR Medical Limited: FDA-registered device maker in Mansfield Nottinghamshire, United Kingdom, 1 510(k) clearance
BPR Medical Limited is registered with the FDA (registration 9681409) in Mansfield Nottinghamshire, United Kingdom. It lists 5 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 13, 2009. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9681409
- FEI number
- 1000509422
- Address
- 22 Hamilton Way Oakham Business Park, Mansfield Nottinghamshire, United Kingdom, NG18 5BU
- Owner or operator
- BPR Medical Ltd (9016353)
- Roles
- Manufacturer, Specification developer
- First device listed
- April 21, 1999
- Registered through
- 2026
- Brand names listed
- FireSafe Cannula Valve, FireSafe Nozzle, Firesafe Nasal Cannula, Microdial Flowmeter, Nitric Oxide Pressure Regulator, Oxygen Demand Valve, Thermal Fuse Cover
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cannula, Nasal, Oxygen | CAT | 1 | Manufacturer | accessdata.fda.gov |
| Flowmeter, Tube, Thorpe, Back-Pressure Compensated | CAX | 1 | Manufacturer, Specification developer | accessdata.fda.gov |
| Regulator, Pressure, Gas Cylinder | CAN | 1 | Manufacturer | accessdata.fda.gov |
| Tube, Thorpe, Uncompensated | BYM | 1 | Manufacturer | accessdata.fda.gov |
| Valve, Non-Rebreathing | CBP | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| March 13, 2009 | K082345 | OXYGEN DEMAND VALVE | CBP | Substantially Equivalent | Bpr Medical, Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Flowmeter, Tube, Thorpe, Back-Pressure Compensated
- All makers of Regulator, Pressure, Gas Cylinder
- All makers of Valve, Non-Rebreathing
- All makers of Cannula, Nasal, Oxygen
- All makers of Tube, Thorpe, Uncompensated
Updated March 13, 2009. 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.