Saphenous Vein Distention System

Saphenous Vein Distention System - 200mmHg - Sterile

Registry build 21.09.26
3manufacturers in China registered for this device type
2catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Guangdong (2), Jiangsu (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code DWF
Manufacturer City Province Registered as Device types
Gcmedica Enterprise Ltd.(Wuxi) Wuxi Jiangsu Contract manufacturer 55
Modern Medical Equipment Manufacturing Ltd. Heng Li, Dongguan Guangdong Contract manufacturer 26
Modern Medical Equipment Manufacturing (Qing Yuan) Ltd Qing Yuan Guangdong Contract manufacturer 26

Record

Regulatory record for Saphenous Vein Distention System
Listed by DMC Medical Ltd., Ireland
FDA product code DWF
Device type Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
Device class Class 2
Regulation 21 CFR 870.4210
Establishment Specification developer, Manufacturer, Exporter
510(k) K000704
Record published 2016-08-10
Record revised 2026-07-13 (version 4)

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
Packaging Pack of 3, pack of 5

Catalogue Numbers

Catalogue numbers for Saphenous Vein Distention System
Catalogue number Size Status
SVDS200 SAPHENOUS VEIN DISTENTION SYSTEM – 200mmHg In distribution
SVDS300 SAPHENOUS VEIN DISTENTION SYSTEM – 300mmHg In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass Medtronic, Inc. 5,237
DLP™ Medtronic, Inc. 804
Bio-Medicus™ Medtronic, Inc. 223
Pemco Inc Pemco, Inc. 137
Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass Maquet Cardiopulmonary GmbH 135
Venous cardiopulmonary bypass cannula LivaNova USA, Inc. 97
Eopa™ Medtronic, Inc. 87
Surge Cardiovascular MED Michigan Holdings LLC 80
Arterial cardiopulmonary bypass cannula LivaNova USA, Inc. 79
MC2™ Medtronic, Inc. 66
Select Series® Medtronic, Inc. 63
Edwards Lifesciences Aortic Perfusion Cannula Edwards Lifesciences Technology Sarl 52

Showing 12 of 372. All products under Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K992932 2000-06-07

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