Gibeck Respiration
Country not established
- Devices
- 6
What Gibeck Respiration makes
Gibeck Respiration manufactures respiratory care devices, including heated humidifiers for ventilators (e.g., HUMID-VENT 2 S FLEX, HUMID-VENT 2 PORT), portable humidifier systems (e.g., HUMID-VENT MINI), and filter systems for respiratory circuits (e.g., HUMID-VENT FILTER). The company also produces tracheostomy ventilation devices, such as the STOM-VENT, designed for patients requiring long-term mechanical ventilation.
The company’s respiratory devices are classified as Class I under FDA regulations, with relevant products listed via the 510(k) pathway. These devices are intended for use in the United States, where Gibeck Respiration is based.
Catalogue
Humid-Vent 2 S Flex Ref K881656
Regimes: 510(k) Registry: 510(k)Humid-Vent(R) 2 Port Ref K873768
Regimes: 510(k) Registry: 510(k)Humid-Vent Filter Ref K881657
Regimes: 510(k) Registry: 510(k)Humid-Vent 2 S Ref K881644
Regimes: 510(k) Registry: 510(k)Humid-Vent(R) Mini Ref K873767
Regimes: 510(k) Registry: 510(k)Stom-Vent Ref K872153
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gibeck Respiration have in the registry?
The registry currently lists 6 devices for Gibeck Respiration. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gibeck Respiration's devices?
Among its 6 most recently registered devices, Gibeck Respiration has devices listed in FDA 510(k) (6 devices).
What risk classes do Gibeck Respiration's devices fall under?
Among its 6 most recently registered devices, the classes recorded for Gibeck Respiration's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Gibeck Respiration in the registry?
The most recently registered devices listed for Gibeck Respiration include HUMID-VENT 2 S FLEX, HUMID-VENT(R) 2 PORT, HUMID-VENT FILTER and HUMID-VENT 2 S.