Partnership Medical Limited
United KingdomFDA applicant, unverified
- Devices
- 2
What Partnership Medical Limited makes
Partnership Medical Limited manufactures bronchoscopy accessories, including the ScopeFlow Pure™, a disposable irrigation system for airway management, and the EndoStream™, a flexible suction catheter designed for endoscopic procedures.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
ScopeFlow Pure(TM) Ref K181418
Regimes: 510(k) Registry: 510(k)EndoStream(TM) Ref K181457
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Partnership Medical Limited have in the registry?
The registry currently lists 2 devices for Partnership Medical Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Partnership Medical Limited's devices?
Among its 2 most recently registered devices, Partnership Medical Limited has devices listed in FDA 510(k) (2 devices).
What risk classes do Partnership Medical Limited's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Partnership Medical Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Partnership Medical Limited in the registry?
The most recently registered devices listed for Partnership Medical Limited include ScopeFlow Pure(TM) and EndoStream(TM).