Shockwave CS Guide Catheter

The Shockwave CS Guide Catheter provides access to the coronary venous system and a passage for interventional or diagnostic devices. The 9 French catheter may be used alone or as part of a…

Registry build 21.09.26

The Shockwave CS Guide Catheter provides access to the coronary venous system and a passage for interventional or diagnostic devices. The 9 French catheter may be used alone or as part of a dual catheter delivery arrangement. Its single lumen supports introduction of compatible devices into the veins.

A curved distal shaft and radiopaque tip support positioning. The catheter becomes progressively more flexible toward its tip. At the proximal end, a standard luer fitting connects to a hemostasis valve, and a curve indicator provides a visual and tactile reference for the direction of the distal curve.

Listed Item

The Shockwave CS Guide Catheter is a single lumen 9F catheter consisting of a PTFE liner, stainless steel braid, and polymer outer jacket. The transition segments of the catheter have a gradual decrease in stiffness starting from the proximal shaft segment and ending at the distal tip. The Shockwave CS Guide Catheter features a pre-shaped curved distal shaft with radiopaque tip. The proximal end of the guide catheter has a standard luer fitting for connecting to a hemostasis valve. The proximal luer also includes a curve indicator to match the direction of the guide catheter tip curvature and provides a tactile and visual cue to the user.

Construction and Supply

The catheter has a PTFE liner, stainless steel braid and polymer outer jacket. It is supplied sterile following ethylene oxide sterilization and is intended for one use.

14manufacturers in China registered for this device type
1catalogue number
1510(k) clearance

Who Else Makes It

Concentrated in Shanghai (5), Jiangsu (5), Guangdong (3). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code DQY
Manufacturer City Province Registered as Device types
Jabil Circuit (Shanghai) Ltd. Shanghai Shanghai Contract manufacturer 31
Covidien Medical Products (Shanghai) Manufacturing LLC Shanghai Shanghai Contract manufacturer 8
Sterigenics Shanghai ETO Ltd. Shanghai Shanghai Contract manufacturer 65
Steris Sterilization Technologies (Suzhou) Ltd Suzhou Jiangsu Contract manufacturer 44
Goals Sterilization Co., Ltd. Jiaxing Zhejiang Contract manufacturer 26
Wuxi Goals Medical Technology Co., Ltd. Yixing Jiangsu Contract manufacturer 24
Suzhou Zenith Vascular Scitech Limited Suzhou Jiangsu Manufacturer 6
Haolang Technology (Foshan) Limited Corporation Foshan Guangdong Contract manufacturer 6
OrbusNeich Medical (Shenzhen) Co., Ltd. Shenzhen Guangdong Complaint-file establishment 5
Curatia Medical Limited Suzhou Jiangsu Specification developer 5
Shanghai Wallaby Medical Technologies Co., Inc. Shanghai Shanghai Contract manufacturer 5
DK Medical Technology Co., Ltd. Suzhou Jiangsu Manufacturer 3

Showing 12 of 14. All 14 manufacturers in China registered for Catheter, Percutaneous

Record

Regulatory record for Shockwave CS Guide Catheter
Listed by Shockwave Medical, Inc., United States
FDA product code DQY
Device type Catheter, Percutaneous
Device class Class 2
Regulation 21 CFR 870.1250
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K243757
Record published 2025-06-02

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Storage Special storage condition: Store the Shockwave CS Guide Catheter in a cool, dark, dry place.
Sizes Outer diameter 3.1 mm; lumen/inner diameter 2.59 mm; catheter working length 61 cm; introducer sheath compatibility 9 Fr

Catalogue Numbers

Catalogue numbers for Shockwave CS Guide Catheter
Catalogue number Size Status
Shockwave CS Guide Catheter Outer Diameter 3.1 mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
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Z2 Medtronic, Inc. 955
Vista Brite TIP Cordis Corp. 789
Mach1™ Boston Scientific Corporation 777
Sherpa NX Active Medtronic, Inc. 571
Zuma® Medtronic, Inc. 569
Convey Pendracare International B.V. 532
Taiga Medtronic, Inc. 307
RunWay™ Boston Scientific Corporation 300
ConcierGE Guiding Excellence™ Merit Medical Systems, Inc. 295

Showing 12 of 500. All products under Catheter, Percutaneous

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K243757 2025-05-02

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer