Ursus Konsult AB
Country not established
- Devices
- 1
What Ursus Konsult AB makes
Ursus Konsult AB manufactures the TROTEX II Screw Needle Biopsy Instrument Set, a device designed for core needle biopsy procedures to obtain tissue samples for diagnostic evaluation.
The TROTEX II Screw Needle Biopsy Instrument Set is classified as a Class I medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Trotex Ii Screw Needle Biopsy Instr. Set Ref K792316
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ursus Konsult AB have in the registry?
The registry currently lists 1 device for Ursus Konsult AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ursus Konsult AB's devices?
Among its 1 most recently registered device, Ursus Konsult AB has devices listed in FDA 510(k) (1 device).
What risk classes do Ursus Konsult AB's devices fall under?
Among its 1 most recently registered device, the classes recorded for Ursus Konsult AB's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Ursus Konsult AB in the registry?
The most recently registered devices listed for Ursus Konsult AB include TROTEX II SCREW NEEDLE BIOPSY INSTR. SET.