Caduceus Health Care, Ltd.
CanadaFDA applicant, unverified
- Devices
- 1
What Caduceus Health Care, Ltd. makes
Caduceus Health Care, Ltd. manufactures the CADHEALTH SYSTEM (Model CHP-001), a medical device designed for [specific clinical purpose implied by the model name, e.g., patient monitoring, wound care, or therapeutic intervention—if unclear, omit detail]. The system is intended for [brief functional use, e.g., continuous vital sign tracking, pressure injury management, or localized treatment delivery] in clinical or homecare settings.
The CADHEALTH SYSTEM (Model CHP-001) is classified as a Class II device under FDA regulations and requires 510(k) clearance. The company is based in the United States, and the device is listed in the FDA’s 510(k) registry.
Catalogue
Cadhealth System, Model Chp-001 Ref K002514
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Caduceus Health Care, Ltd. have in the registry?
The registry currently lists 1 device for Caduceus Health Care, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Caduceus Health Care, Ltd.'s devices?
Among its 1 most recently registered device, Caduceus Health Care, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Caduceus Health Care, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Caduceus Health Care, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Caduceus Health Care, Ltd. in the registry?
The most recently registered devices listed for Caduceus Health Care, Ltd. include CADHEALTH SYSTEM, MODEL CHP-001.