Tigran Technologies AB
SwedenFDA applicant, unverified
- Devices
- 1
What Tigran Technologies AB makes
Tigran Technologies AB manufactures the TIGRAN PERIBRUSH, a device designed for peribronchial or bronchial brushing procedures, typically used in diagnostic bronchoscopy to collect tissue samples from the airways.
The TIGRAN PERIBRUSH is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Tigran Peribrush Ref K121114
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tigran Technologies AB have in the registry?
The registry currently lists 1 device for Tigran Technologies AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tigran Technologies AB's devices?
Among its 1 most recently registered device, Tigran Technologies AB has devices listed in FDA 510(k) (1 device).
What risk classes do Tigran Technologies AB's devices fall under?
Among its 1 most recently registered device, the classes recorded for Tigran Technologies AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tigran Technologies AB in the registry?
The most recently registered devices listed for Tigran Technologies AB include TIGRAN PERIBRUSH.