Airlife, Inc.
United StatesFDA applicant, unverified
- Devices
- 2,388
What Airlife, Inc. makes
Airlife, Inc. manufactures single-use anaesthesia and ventilator breathing circuits, manual pulmonary resuscitators, reusable electrocardiographic lead sets, and single-use connectors for respiratory support. Their portfolio also includes benchtop therapeutic agent nebulizers, single-use cardiopulmonary resuscitation kits, and single-use electrocardiographic electrodes.
These devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s UDI (Unique Device Identification) database. The company is based in the United States.
Catalogue
Search and filter all 2,388 devicesShowing 1-50 of 2,388
Frequently asked questions
How many devices does Airlife, Inc. have in the registry?
The registry currently lists 2388 devices for Airlife, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Airlife, Inc.'s devices?
Among its 50 most recently registered devices, Airlife, Inc. has devices listed in FDA 510(k) (2 devices) and FDA GUDID (48 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Airlife, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Airlife, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Airlife, Inc. in the registry?
The most recently registered devices listed for Airlife, Inc. include AirLife 37740CE, Air Life AM-2000, Air Life AM-2100 and Air Life AM-2200.