Berchtold GmbH & Co. KG
Country not established
- Devices
- 3
What Berchtold GmbH & Co. KG makes
Berchtold GmbH & Co. KG manufactures the CHROMOPHARE F 628 and F 528, as well as the CHROMOPHARE E 668, which are designed for medical illumination purposes, likely in surgical or procedural settings.
These devices fall under FDA Class II regulation and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Chromophare F 628 And F 528 Ref K120392
Regimes: 510(k) Registry: 510(k)Berchtold Elektrotom 106 Hitt Ref K013668
Regimes: 510(k) Registry: 510(k)Chromophare E 668 Ref K090378
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Berchtold GmbH & Co. KG have in the registry?
The registry currently lists 3 devices for Berchtold GmbH & Co. KG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Berchtold GmbH & Co. KG's devices?
Among its 3 most recently registered devices, Berchtold GmbH & Co. KG has devices listed in FDA 510(k) (3 devices).
What risk classes do Berchtold GmbH & Co. KG's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Berchtold GmbH & Co. KG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Berchtold GmbH & Co. KG in the registry?
The most recently registered devices listed for Berchtold GmbH & Co. KG include CHROMOPHARE F 628 AND F 528, BERCHTOLD ELEKTROTOM 106 HITT and CHROMOPHARE E 668.