Blackbriar Regulatory Services, LLC
Country not established
- Devices
- 4
What Blackbriar Regulatory Services, LLC makes
Blackbriar Regulatory Services, LLC makes single-use surgical and medical face masks, including procedure masks with ear loops in various filtration levels such as Level 1, Level 2, and Level 3, as well as multi-layer procedure masks.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) and FDA UDI registries; the company is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
BRS Procedure Face Mask Ref K202824
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 117425172
Frequently asked questions
How many devices does Blackbriar Regulatory Services, LLC have in the registry?
The registry currently lists 4 devices for Blackbriar Regulatory Services, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Blackbriar Regulatory Services, LLC's devices?
Among its 4 most recently registered devices, Blackbriar Regulatory Services, LLC has devices listed in FDA 510(k) (1 device) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Blackbriar Regulatory Services, LLC's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Blackbriar Regulatory Services, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Blackbriar Regulatory Services, LLC in the registry?
The most recently registered devices listed for Blackbriar Regulatory Services, LLC include BRS Level 1 Procedure Face Mask with Ear Loops 850021617004, BRS Level 3 Procedure Face Mask - 3 Layers 850021617561, BRS Level 2 Procedure Mask with Ear Loops 850021617196 and BRS Procedure Face Mask.