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Sign in to claim this brandTerumo Clinical Supply Co., Ltd.
US
Last updated May 27, 2026
What Terumo Clinical Supply Co., Ltd. makes
Terumo Clinical Supply manufactures vascular microcatheters and thrombectomy suction catheters, including models like the Progreat Lambda and PRIORITYONE. These devices are designed for interventional radiology and neurovascular procedures, facilitating precise catheterization and clot removal in vascular applications.
The company’s products are regulated as Class II medical devices in the US, with authorisations granted through FDA 510(k) submissions and listed under the FDA’s Unique Device Identification (UDI) system. The manufacturer operates from the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Terumo Clinical Supply Co., Ltd. manufacture?
Terumo Clinical Supply Co., Ltd. specializes in vascular microcatheters and thrombectomy suction catheters. These devices are primarily used in interventional radiology and neurovascular procedures to enable precise catheterization and the removal of blood clots within blood vessels. Examples of their products include the Progreat Lambda and PRIORITYONE.
Where is Terumo Clinical Supply Co., Ltd. based?
The company is based in the United States. While the specific location within the country is not detailed, the headquarters or primary operations are established there.
Which regulatory registries or databases list Terumo Clinical Supply’s devices?
Terumo Clinical Supply’s devices are listed in the FDA’s 510(k) premarket notification registry and the FDA’s Unique Device Identification (UDI) system. These registries track the authorisation status and identification details of Class II medical devices in the US.
How are Terumo Clinical Supply’s devices classified in the US?
Terumo Clinical Supply’s devices are classified as Class II medical devices in the US. This classification applies to products that generally pose moderate risk and require special controls to ensure their safety and effectiveness, such as vascular catheters and thrombectomy tools.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- terumomedical.com
- —
- —
- [email protected]
- Phone
- +1(800)283-7866
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 691034748
Catalogue (11)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Progreat Lambda | CC-MC915SN | FDA UDI | Class II | Active |
| Progreat Lambda | CC*M1916AN | FDA UDI | Class II | Active |
| Priorityone | UG1652 | FDA UDI | Class II | Active |
| Progreat Lambda | CC-MC913DN | FDA UDI | Class II | Active |
| Priorityone | UG1602 | FDA UDI | Class II | Active |
| Progreat Lambda | CC-MC915AN | FDA UDI | Class II | Active |
| Progreat Lambda | CC-MC913SN | FDA UDI | Class II | Active |
| Progreat Lambda | CC*M1916SN | FDA UDI | Class II | Active |
| Progreat Lambda | CC-MC915DN | FDA UDI | Class II | Active |
| Progreat Lambda | CC*M1916DN | FDA UDI | Class II | Active |
| Progreat Lambda | K211078 | FDA 510(k)FDA UDI | Class II | Active |
Related Companies
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Authorities
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Terumo Clinical Supply Co., Ltd. Kakamigahara Gifu · JP FEI 3009500972