Hi Tec Medical Vertriebs-GmbH Fur Innovative Mediz
GermanyFDA applicant, unverified
- Devices
- 2
What Hi Tec Medical Vertriebs-GmbH Fur Innovative Mediz makes
Hi Tec Medical Vertriebs-GmbH manufactures CO₂ insufflators, including the Type 1300 and 1100 models, designed for medical insufflation procedures.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
Hi-Tec CO2 Insufflator Type 1300 Ref K955477
Regimes: 510(k) Registry: 510(k)CO2 Insufflator 1100 Ref K930013
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hi Tec Medical Vertriebs-GmbH Fur Innovative Mediz have in the registry?
The registry currently lists 2 devices for Hi Tec Medical Vertriebs-GmbH Fur Innovative Mediz. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hi Tec Medical Vertriebs-GmbH Fur Innovative Mediz's devices?
Among its 2 most recently registered devices, Hi Tec Medical Vertriebs-GmbH Fur Innovative Mediz has devices listed in FDA 510(k) (2 devices).
What risk classes do Hi Tec Medical Vertriebs-GmbH Fur Innovative Mediz's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Hi Tec Medical Vertriebs-GmbH Fur Innovative Mediz's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hi Tec Medical Vertriebs-GmbH Fur Innovative Mediz in the registry?
The most recently registered devices listed for Hi Tec Medical Vertriebs-GmbH Fur Innovative Mediz include HI-TEC CO2 INSUFFLATOR TYPE 1300 and CO2 INSUFFLATOR 1100.