LiquID 071

The LiquID 071 is a guide catheter extension used with a conventional guide catheter to reach selected regions of the coronary or peripheral vasculature and help place interventional…

Registry build 21.09.26

The LiquID 071 is a guide catheter extension used with a conventional guide catheter to reach selected regions of the coronary or peripheral vasculature and help place interventional devices. This configuration fits within a 7F guide catheter. It advances through the guide catheter and beyond its distal tip.

A proximal stainless steel shaft connects to a single-lumen distal segment through which interventional devices pass. The distal segment has a PTFE liner, a metal support coil with a tantalum core and an outer nylon-based polymer layer. Its rounded tip incorporates PTFE and Pebax.

Length and Positioning

The device has a 150 cm working length and a 15 cm distal exchange segment. Proximal shaft marks are located approximately 95 and 105 cm from the distal tip to assist positioning.

14manufacturers in China registered for this device type
2catalogue numbers in this listing
2510(k) clearances naming this product code

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 LiquID 071
Listed by Seigla Medical, Inc., United States
FDA product code DQY
Device type Catheter, Percutaneous
Device class Class 2
Regulation 21 CFR 870.1250
Establishment Manufacturer
510(k) K220691
Record published 2023-07-14
Record revised 2025-11-11 (version 2)

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
Sizes Catheter gauge 7 Fr
Distribution end date 2025-06-01

Catalogue Numbers

Catalogue numbers for LiquID 071
Catalogue number Size Status
7F Catheter Gauge 7 Fr In distribution
7F Catheter Gauge 7 Fr Withdrawn

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
K243691 2025-04-04
K220691 2022-05-05

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