Catapult Guide Sheath

Introducer Sheath System containing One (1) introducer Sheath with haemostasis valve and Two (2) dilators. Introducer Sheath is hydrophilic coated on the distal end.

Registry build 21.09.26
13manufacturers in China registered for this device type
39catalogue numbers in this listing
8510(k) clearances naming this product code
1recall

Who Else Makes It

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

Chinese manufacturers registered for FDA product code DYB
Manufacturer City Province Registered as Device types
Mehow Innovative (Huizhou) Ltd. Huizhou Guangdong Contract manufacturer 11
Tianjin Demax Medical Technology Co., Ltd. Tianjin Tianjin Contract manufacturer 5
Steris Sterilization Technologies (Suzhou) Ltd Suzhou Jiangsu Contract manufacturer 44
Shanghai INT Medical Instruments Co., Ltd. Shanghai Shanghai Contract manufacturer 10
Lepu Medical Technology (Beijing) Co., Ltd. Beijing Beijing Manufacturer 7
Beijing Target Medical Technologies Inc. Beijing Beijing Contract manufacturer 7
Beijing Demax Medical Technology Co., Ltd. Beijing Beijing Manufacturer 5
Curatia Medical Limited Suzhou Jiangsu Specification developer 5
Tianjin Ethylene Oxide Sterilization Technology Co., Ltd. Tianjin Tianjin Contract manufacturer 4
Shanghai Microport EP Medtech Co., Ltd. Shanghai Shanghai Manufacturer 3
Becton Dickinson Medical Devices Co., Ltd. Suzhou Suzhou Jiangsu Contract manufacturer 2
Cardiocycle Medical(Suzhou) Co., Ltd. Suzhou Jiangsu Complaint-file establishment 1

Showing 12 of 13. All 13 manufacturers in China registered for Introducer, Catheter

Record

Regulatory record for Catapult Guide Sheath
Listed by Contract Medical International GmbH, Germany
FDA product code DYB
Device type Introducer, Catheter
Device class Class 2
Regulation 21 CFR 870.1340
Establishment Contract manufacturer, Manufacturer
Record published 2023-09-01
Record revised 2026-07-27 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Latex Labelled latex-free
Label carries lot or batch number, expiry date
Storage Special storage condition: Keep dry, Keep away from direct sunlight
Packaging Packer of 5, corrugate
Sizes Length 15 to 130 cm; catheter inner diameter 1.6 to 2.88 mm; catheter inner diameter 1.92 cm

Catalogue Numbers

Catalogue numbers for Catapult Guide Sheath
Catalogue number Size Status
4F, 60cm, straight, hydrophilic coated Length 60 cm In distribution
6F, 90cm, straight, hydrophilic coated Length 90 cm In distribution
5F, 45cm, RDC, hydrophilic coated Length 45 cm In distribution
5F, 130cm, Straight, hydrophilic coated Length 130 cm In distribution
6F, 45cm, Multipurpose, hydrophilic coated Length 45 cm In distribution
6F, 130cm, Straight, hydrophilic coated Length 130 cm In distribution
7F, 15cm, straight, hydrophilic coated Length 15 cm In distribution
6F, 90cm, RDC, hydrophilic coated Length 90 cm In distribution
4F, 90cm, straight, hydrophilic coated Length 90 cm In distribution
7F, 90cm, Hockey stick, hydrophilic coated Length 90 cm In distribution
8F, 15cm, straight, hydrophilic coated Length 15 cm In distribution
4F, 45cm, straight, hydrophilic coated Length 45 cm In distribution
6F, 45cm, LIMA, hydrophilic coated Length 45 cm In distribution
7F, 45cm, straight, hydrophilic coated Length 45 cm In distribution
7F, 90cm, Multipurpose, hydrophilic coated Length 90 cm In distribution
6F, 45cm, RDC, hydrophilic coated Length 45 cm In distribution
7F, 60cm, straight, hydrophilic coated Length 60 cm In distribution
8F, 90cm, straight, hydrophilic coated Length 90 cm In distribution
8F, 45cm, straight, hydrophilic coated Length 45 cm In distribution
6F, 90cm, Hockey stick, hydrophilic coated Length 90 cm In distribution
5F, 45cm, straight, hydrophilic coated Length 45 cm In distribution
7F, 90cm, straight, hydrophilic coated Length 90 cm In distribution
5F, 45cm, Hockey stick, hydrophilic coated Length 45 cm In distribution
6F, 45cm, straight, hydrophilic coated Length 45 cm In distribution
7F, 45cm, Hockey stick, hydrophilic coated Length 45 cm In distribution
6F, 60cm, straight, hydrophilic coated Length 60 cm In distribution
7F, 45cm, Multipurpose, hydrophilic coated Length 45 cm In distribution
5F, 15cm, straight, hydrophilic coated Length 15 cm In distribution
5F, 45cm, Multipurpose, hydrophilic coated Length 45 cm In distribution
6F, 15cm, straight, hydrophilic coated Length 15 cm In distribution
6F, 90cm, Multipurpose, hydrophilic coated Length 90 cm In distribution
4F, 130cm, Straight, hydrophilic coated Length 130 cm In distribution
6F, 45cm, Hockey stick, hydrophilic coated Length 45 cm In distribution
5F, 60cm, straight, hydrophilic coated Length 60 cm In distribution
8F, 60cm, straight, hydrophilic coated Length 60 cm In distribution
7F, 45cm, LIMA, hydrophilic coated Length 45 cm In distribution
5F, 90cm, straight, hydrophilic coated Length 90 cm In distribution
7F, 45cm, RDC, hydrophilic coated Length 45 cm In distribution
4F, 15cm, straight, hydrophilic coated Length 15 cm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Demax Beijing Demax Medical Technology Co., Ltd. 2,841
Arrow Teleflex Medical LLC 1,036
Prelude IDeal™ Merit Medical Systems, Inc. 294
Fast-Cath™ St. Jude Medical 213
Flexor Cook Incorporated 182
Prelude Ease™ Merit Medical Systems, Inc. 176
Performer Cook Incorporated 174
VSI Teleflex Medical LLC 154
Peel-Away Cook Incorporated 153
OptiSeal™ Greatbatch Medical 127
Brilliant Lepu Medical Technology (Beijing) Co., Ltd. 122
Super Sheath Togo Medikit Co., Ltd. 122

Showing 12 of 439. All products under Introducer, Catheter

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K250439 2025-03-16
K240957 2024-08-14
K221914 2022-07-29
K203179 2020-11-20
K181463 2018-12-13
K153197 2016-01-11
K142357 2015-06-25
K100799 2011-02-25

Recalls

1 of these is Class II. Class II means a temporary or reversible health consequence. 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
2025-07-30 Class II Under Investigation by firm Units may have been packaged with an incorrect pouch label, which lists the reference number and unique device identifier of the 4F version of the device, rather than the packaged 6F version. 2500

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