Inditherm Medical
Country not established
- Devices
- 2
What Inditherm Medical makes
Inditherm Medical manufactures patient warming systems, including active and passive models designed for intraoperative and critical care settings. The portfolio includes systems for general surgery, cardiac surgery, neonatal care, and intensive care units, with features for temperature monitoring and controlled warming.
The company’s devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. Products are intended for use in the United States, where compliance with FDA requirements is mandatory. No additional registries or international authorisations are referenced.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Cosytherm, Models NCM1, NCM2, NCB1, CCU1, CRU1 Ref K061902
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Inditherm Medical have in the registry?
The registry currently lists 2 devices for Inditherm Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Inditherm Medical's devices?
Among its 2 most recently registered devices, Inditherm Medical has devices listed in FDA 510(k) (2 devices).
What risk classes do Inditherm Medical's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Inditherm Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Inditherm Medical in the registry?
The most recently registered devices listed for Inditherm Medical include INDITHERM PATIENT WARMING SYSTEM, MODELS MECU1; OTM1; OTM2; GTM1; PTM1; OTB; RB1 and COSYTHERM, MODELS NCM1, NCM2, NCB1, CCU1, CRU1.