Bebig Isotopen-Und Medizintechnik GmbH
GermanyFDA applicant, unverified
- Devices
- 3
What Bebig Isotopen-Und Medizintechnik GmbH makes
Bebig Isotopen-Und Medizintechnik GmbH manufactures low‑dose rate brachytherapy products, including the BEBIG ISOSEED I‑125 and ISOSEEDS I‑125 radioactive seeds as well as a brachytherapy strand device for internal radiation treatment.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) database. The company is based in the United States.
Catalogue
Bebig Isoseed I-125 Ref K033781
Regimes: 510(k) Registry: 510(k)Isoseeds I-125 Ref K021343
Regimes: 510(k) Registry: 510(k)Brachytherapy Strand Device Ref K040339
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bebig Isotopen-Und Medizintechnik GmbH have in the registry?
The registry currently lists 3 devices for Bebig Isotopen-Und Medizintechnik GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bebig Isotopen-Und Medizintechnik GmbH's devices?
Among its 3 most recently registered devices, Bebig Isotopen-Und Medizintechnik GmbH has devices listed in FDA 510(k) (3 devices).
What risk classes do Bebig Isotopen-Und Medizintechnik GmbH's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Bebig Isotopen-Und Medizintechnik GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bebig Isotopen-Und Medizintechnik GmbH in the registry?
The most recently registered devices listed for Bebig Isotopen-Und Medizintechnik GmbH include BEBIG ISOSEED I-125, ISOSEEDS I-125 and BRACHYTHERAPY STRAND DEVICE.