Trumpf Kreuzer Medizin Systeme GmbH + Co.Kg
Country not established
- Devices
- 3
What Trumpf Kreuzer Medizin Systeme GmbH + Co.Kg makes
Trumpf Kreuzer Medizin Systeme GmbH + Co.Kg manufactures LED-based medical lighting systems, including the ILED and TRULIGHT 5520/TRULIGHT 5320 models, designed for surgical and procedural environments.
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
- Regimes: 510(k) Registry: 510(k)
Iled Ref K061317
Regimes: 510(k) Registry: 510(k)Trulight 5520 And Trulight 5320 Ref K102758
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Trumpf Kreuzer Medizin Systeme GmbH + Co.Kg have in the registry?
The registry currently lists 3 devices for Trumpf Kreuzer Medizin Systeme GmbH + Co.Kg. Devices recorded under merged duplicate company entries are counted once.
Which registries list Trumpf Kreuzer Medizin Systeme GmbH + Co.Kg's devices?
Among its 3 most recently registered devices, Trumpf Kreuzer Medizin Systeme GmbH + Co.Kg has devices listed in FDA 510(k) (3 devices).
What risk classes do Trumpf Kreuzer Medizin Systeme GmbH + Co.Kg's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Trumpf Kreuzer Medizin Systeme GmbH + Co.Kg's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Trumpf Kreuzer Medizin Systeme GmbH + Co.Kg in the registry?
The most recently registered devices listed for Trumpf Kreuzer Medizin Systeme GmbH + Co.Kg include ILED 3 MOBILE (I300M), TRULIGHT 5500 MOBILE (T500M), TRULIGHT 5300 MOBILE (T300M), ILED and TRULIGHT 5520 AND TRULIGHT 5320.