Carrier™ Delivery Catheter

The Carrier™ Delivery Catheter is a single lumen, variable stiffness, composite catheter. The design facilitates the advancement of the catheter and is intended to assist the delivery of…

Registry build 21.09.26

The Carrier™ Delivery Catheter is a single lumen, variable stiffness, composite catheter. The design facilitates the advancement of the catheter and is intended to assist the delivery of interventional devices in the peripheral and neurovasculature. The outer surface of the Carrier™ Delivery Catheter is coated with a hydrophilic coating to increase lubricity. The proximal end of the Carrier™ Delivery Catheter incorporates a luer fitting for the attachment of accessories. Two radiopaque markers at the distal end help to facilitate fluoroscopic visualization. A Steam Shaping Mandrel and Peel-away Introducer Tube are included within the tray. The Carrier™ Delivery Catheter is provided sterile, non-pyrogenic, and is intended for single use only.

14manufacturers in China registered for this device type
6catalogue numbers in this listing
1510(k) clearance
1recall

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 Carrier™ Delivery Catheter
Listed by Balt USA, LLC, United States
FDA product code DQY
Device type Catheter, Percutaneous
Device class Class 2
Regulation 21 CFR 870.1250
Establishment Complaint-file establishment, Manufacturer
510(k) K230609
Record published 2023-11-07

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, manufacturing date
Storage Special storage condition: Avoid exposure to water, sunlight, extreme temperatures, and high humidity during storage. Store the Carrier Delivery Ca
Sizes Catheter length 152 to 162 cm

Catalogue Numbers

Catalogue numbers for Carrier™ Delivery Catheter
Catalogue number Size Status
CR8081 Catheter Length 152 cm In distribution
CR8081162 Catheter Length 162 cm In distribution
CR7071 Catheter Length 152 cm In distribution
CR7074162 Catheter Length 162 cm In distribution
CR7074 Catheter Length 152 cm In distribution
CR7071162 Catheter Length 162 cm In distribution

Same Product Code

Other products under the same FDA 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

FDA 510(k) clearances naming this product code
Clearance Decision date
K182918 2019-03-21

Recalls

1 of these is Class I. Class I is the FDA’s most serious grade: a reasonable probability of serious injury or death. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity
2025-09-25 Class I Process control Due to an identified manufacturing defect involving coating material lifting within the catheter’s distal inner diameter/lumen. 207 catheters

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