Teleport Glide Microcatheter

Teleport Glide is a microcatheter for guiding and supporting a guidewire in peripheral blood vessels. Its single lumen also permits guidewire exchange and delivery of contrast medium. The…

Registry build 21.09.26

Teleport Glide is a microcatheter for guiding and supporting a guidewire in peripheral blood vessels. Its single lumen also permits guidewire exchange and delivery of contrast medium.

The catheter has a hub, shaft, distal section and radiopaque tip. A hydrophilic polymer coating makes its outer surface more lubricious, while a fluoropolymer lumen lining helps the guidewire move inside.

Length and Guidewire Options

The family offers three sizes, two tip shapes and working lengths of 65, 90, 135, 150, 180 and 200 cm. Depending on the selected catheter, the compatible guidewire is 0.018 inch or 0.035 inch. These options describe different catheter configurations within the peripheral range.

14manufacturers in China registered for this device type
22catalogue numbers in this listing
3510(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 Teleport Glide Microcatheter
Listed by OrbusNeich Medical (Shenzhen) Co., Ltd., China
FDA product code DQY
Device type Catheter, Percutaneous
Device class Class 2
Regulation 21 CFR 870.1250
Establishment Complaint-file establishment, Manufacturer
510(k) K253361
Record published 2026-07-20

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Label carries lot or batch number, expiry date, manufacturing date

Catalogue Numbers

Catalogue numbers for Teleport Glide Microcatheter
Catalogue number Size Status
9218-150-01 In distribution
9235-150-01 In distribution
9235-200-01 In distribution
9218-135-11 In distribution
9235-065-11 In distribution
9235-200-11 In distribution
9235-065-01 In distribution
9218-090-11 In distribution
9218-200-01 In distribution
9218-150-11 In distribution
9218-180-11 In distribution
9218-135-01 In distribution
9235-090-11 In distribution
9235-150-11 In distribution
9218-200-11 In distribution
9235-180-01 In distribution
9218-090-01 In distribution
9218-180-01 In distribution
9235-180-11 In distribution
9235-090-01 In distribution
9235-135-11 In distribution
9235-135-01 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
K253361 2026-04-10
K242588 2025-01-07
K231608 2024-01-07

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