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Sign in to claim this brandTerumo Corp.
US
Last updated May 23, 2026
What Terumo Corp. makes
Terumo Corp. makes a range of medical devices, including guidewires, angiographic catheters, vascular guide-catheters, peripheral artery stents, vascular microcatheters, and extracorporeal membrane oxygenators. These devices are used in various medical procedures, such as cardiac and peripheral vascular interventions. The company's portfolio also includes gastro-urological guidewires and general-purpose non-vascular guidewires.
The company's devices are regulated under Class I, Class II, and Class III classifications and are listed in the FDA's UDI registry. Terumo Corp. is based in the US.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What type of medical devices does Terumo Corp. manufacture?
Terumo Corp. makes guidewires, catheters, stents, and oxygenators, which are used in cardiac, vascular, and other medical procedures, because these devices are listed in the company's device categories.
Where is Terumo Corp. based?
Terumo Corp. is based in the US, as indicated by the company's country listing.
Which regulatory registry lists Terumo Corp.'s devices?
Terumo Corp.'s devices are listed in the FDA's UDI registry, which tracks unique device identifiers for medical devices.
How are Terumo Corp.'s devices classified?
Terumo Corp.'s devices are classified under Class I, Class II, and Class III, which are regulatory classifications that determine the level of control and oversight for medical devices.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
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Catalogue (676)
Page 13 of 14| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Surflash | SR*FNP2032 | FDA UDI | Class II | Unknown |
| Finecross | 35-1450 | FDA UDI | Class II | Active |
| Teruflex Transfer Bag | BB*T015CB70 | FDA UDI | Class II | Active |
| Visiglide2 | G-260-2527A | FDA UDI | Class II | Active |
| Glidesheath Slender | RM*ES7F10HAU | FDA UDI | Class II | Unknown |
| Surflash | SR*FF1651 | FDA UDI | Class II | Active |
| Visiglide2 | G-260-3545A | FDA UDI | Class II | Active |
| Progreat | MC*PV2415ZRC | FDA UDI | Class II | Active |
| Glidecath | CG521 | FDA UDI | Class II | Active |
| Capiox®rx | CX*RX05RW | FDA UDI | Class II | Active |
| Glidewire | GR3802 | FDA UDI | Class II | Active |
| Headliner | GM1222 | FDA UDI | Class II | Active |
| Capiox | CX*FX05REA | FDA UDI | Class II | Active |
| Glidewire | GR3541 | FDA UDI | Class II | Active |
| Capiox® Hemoconcentrator | CX*HC11L | FDA UDI | Class II | Active |
| Glidewire | GS3509 | FDA UDI | Class II | Active |
| Glidecath | CG419 | FDA UDI | Class II | Active |
| Glidewire | EWS4525 | FDA UDI | Class II | Active |
| Capiox | XX*CXH15 | FDA UDI | Class I | Active |
| Glidesheath Slender | RM*ES6J10HAT | FDA UDI | Class II | Unknown |
| Terumo Sampling Site Coupler | TC*MP1 | FDA UDI | Class I | Active |
| Glidewire | RG*GW1818SP | FDA UDI | Class II | Active |
| Visiglide | G-240-2527S | FDA UDI | Class II | Active |
| Progreat | MC*PV2815Y | FDA UDI | Class II | Active |
| Capiox®fx | CX*FX15E | FDA UDI | Class II | Active |
| Optitorque | 40-6061 | FDA UDI | Class II | Active |
| Visiglide | G-240-3545S | FDA UDI | Class II | Active |
| Visiglide2 | G-260-2545A | FDA UDI | Class II | Active |
| Visiglide2 | G-260-3527S | FDA UDI | Class II | Active |
| Capiox®rx | CX*RX15W | FDA UDI | Class II | Active |
| Glidecath | CG431 | FDA UDI | Class II | Active |
| Visiglide2 | G-260-2527S | FDA UDI | Class II | Active |
| Optitorque | 40-5013 | FDA UDI | Class II | Active |
| Capiox®fx | CX*FX05W | FDA UDI | Class II | Active |
| Glidecath | RF*WA25110M | FDA UDI | Class II | Active |
| Optitorque | 40-6013 | FDA UDI | Class II | Active |
| Optitorque | 40-5045 | FDA UDI | Class II | Active |
| Glidecath | CG416 | FDA UDI | Class II | Active |
| Optitorque | 40-5022 | FDA UDI | Class II | Active |
| Runthrough | 25-5011 | FDA UDI | Class II | Active |
| Capiox®rx | CX*RX15E | FDA UDI | Class II | Active |
| Capiox®rx | CX*RX15RW40 | FDA UDI | Class II | Active |
| Cardiopulmonary Bypass Pump Tubing - 1/4 Inch Tubing, Cardiopulmonary Bypass Pump Tubing - 3/8 Inch Tubing | K993189 | FDA 510(k) | Class II | Active |
| Foundation | K040783 | FDA 510(k) | Class II | Active |
| Single Use Guidewire, Models G-240-2527s, G-240-2545s, G-240-2527a, G-240-2545a, G-240-3527s, G-240-3545s & G-240-3527a | K091417 | FDA 510(k) | Class II | Active |
| Terumo Digital Blood Pressure Monitor Es-H55a | K071075 | FDA 510(k) | Class II | Active |
| Pen Injector Needle 32.5 | K250700 | FDA 510(k) | Class II | Active |
| Capiox Fx15 And Fx25 Hollow Fiber Oxygenator And Arterial Filter | K071494 | FDA 510(k) | Class II | Active |
| Terumo Surshield Safety I.v. Catheter (18g X 51mm & 20g X 51mm Sizes) | K090973 | FDA 510(k) | Class II | Active |
| Glidesheath | K033681 | FDA 510(k) | Class II | Active |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Terumo Corp. SHIBUYA-KU, TOKYO · JP FEI 2828