CPS Locator 3d Plus Delivery Catheter
CPS Locator 3D Plus Delivery Catheter introduces catheters or pacing and defibrillation leads through venous access. It is supplied with a dilator and Luer cap and has a proximal hemostatic…
CPS Locator 3D Plus Delivery Catheter introduces catheters or pacing and defibrillation leads through venous access. It is supplied with a dilator and Luer cap and has a proximal hemostatic valve.
The braid-reinforced Pebax shaft has a hydrophilic liner and a soft rounded radiopaque distal tip. It accepts a 0.035-inch guidewire, with 42 or 45 cm working lengths.
Listed Item
The Delivery Catheter is indicated for the introduction of various types of catheters and pacing or defibrillation leads.
Lumen and Removal
The subject catheter has a 10.2 Fr outer diameter and an 8.4 Fr inner diameter. After lead or catheter placement, the delivery catheter can be slit for removal. Devices are sterilized by electron beam for single-patient use.
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.
| 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
| Listed by | Centerpoint Systems LLC, United States |
|---|---|
| FDA product code | DQY |
| Device type | Catheter, Percutaneous |
| Device class | Class 2 |
| Regulation | 21 CFR 870.1250 |
| Establishment | Contract manufacturer, Complaint-file establishment, Manufacturer |
| 510(k) | K250828 |
| Record published | 2025-07-07 |
| Record revised | 2025-10-24 (version 2) |
Specifications
| MRI safety | MR Unsafe |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, expiry date |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| DS4D200-45 | In distribution | |
| DS4D200-42 | In distribution | |
| DS2D400-45 | In distribution | |
| DS4D400-42 | In distribution | |
| DS4D300-45 | In distribution | |
| DS4D300-42 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Launcher™ | Medtronic, Inc. | 3,805 |
| Sherpa NX Balanced™ | Medtronic, Inc. | 1,523 |
| Arrow | Teleflex Medical LLC | 1,249 |
| 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
| Clearance | Decision date |
|---|---|
| K261766 | 2026-07-29 |
| K262240 | 2026-07-29 |
| K250147 | 2025-08-22 |
| K250828 | 2025-06-27 |
| K250492 | 2025-06-18 |
| K243180 | 2024-12-04 |
| K230363 | 2023-03-09 |
| K210009 | 2021-11-24 |
| K190475 | 2019-06-28 |
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.