Riken Keiki Co., Ltd.
Country not established
- Devices
- 2
What Riken Keiki Co., Ltd. makes
Riken Keiki Co., Ltd. manufactures devices for testing and monitoring anaesthesia vaporizers, including gas indicators and dedicated testers. Their portfolio includes models like the RIKEN GAS INDICATOR (1806H, 1802D, IF-18), designed to verify the performance and safety of anaesthetic delivery systems in clinical settings.
These devices are classified as Class II under regulatory frameworks and are listed in the FDA’s 510(k) and UDI registries. The company operates with a US presence, adhering to applicable medical device regulations for their authorised products.
Catalogue
- Registry: GUDID
- Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 690573670
Frequently asked questions
How many devices does Riken Keiki Co., Ltd. have in the registry?
The registry currently lists 2 devices for Riken Keiki Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Riken Keiki Co., Ltd.'s devices?
Among its 2 most recently registered devices, Riken Keiki Co., Ltd. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Riken Keiki Co., Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Riken Keiki Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Riken Keiki Co., Ltd. in the registry?
The most recently registered devices listed for Riken Keiki Co., Ltd. include RIKEN KEIKI Co., Ltd. FI-8000 and RIKEN GAS INDICATOR (3 MODELS, 1806H, 1802D, IF-18).