Kimble-Terumo, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Kimble-Terumo, Inc. makes
Kimble-Terumo, Inc. manufactures blood sampling kits, including the PREZAPAK L Arterial Blood Sampling Kit, and automated blood collection systems like the VENOJECT AUTOSEP. These products are designed for clinical and laboratory use to facilitate safe and efficient blood collection procedures.
The company’s portfolio is regulated under Class II medical devices in the US, with devices authorised via the FDA’s 510(k) pathway. Products are listed in the FDA’s 510(k) registry, reflecting compliance with US regulatory requirements.
Catalogue
Prezapak L Arterial Blood Sampling Kit Ref K801015
Regimes: 510(k) Registry: 510(k)Venoject Autosep Ref K792587
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kimble-Terumo, Inc. have in the registry?
The registry currently lists 2 devices for Kimble-Terumo, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kimble-Terumo, Inc.'s devices?
Among its 2 most recently registered devices, Kimble-Terumo, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Kimble-Terumo, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Kimble-Terumo, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kimble-Terumo, Inc. in the registry?
The most recently registered devices listed for Kimble-Terumo, Inc. include PREZAPAK L ARTERIAL BLOOD SAMPLING KIT and VENOJECT AUTOSEP.