Duoglide

Short-Term Dialysis Catheter

Registry build 21.09.26
1manufacturer
24catalogue numbers in this listing
3recalls on this code

Who Else Makes It

Registered in Guangdong.

Chinese manufacturers registered for FDA product code MPB
Manufacturer City Province Registered as Device types
Guangdong Baihe Medical Technology Co., Ltd. Foshan Guangdong Contract manufacturer 4

Record

Regulatory record for Duoglide
Listed by Bard Access Systems, Inc., United States
FDA product code MPB
Device type Catheter, Hemodialysis, Non-Implanted
Device class Class 2
Regulation 21 CFR 876.5540
Establishment Specification developer, Complaint-file establishment, Manufacturer, Exporter
Record published 2026-04-13

Specifications

Specifications
MRI safety MR Safe
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 Storage environment temperature 20 to 25 °C
Packaging Case of 5
Sizes Catheter gauge 13 Fr; length 12.5 to 30 cm

Catalogue Numbers

Catalogue numbers for Duoglide
Catalogue number Size Status
5887200B Catheter Gauge 13 Fr In distribution
5887120M Length 12.5 cm In distribution
5887240B Catheter Gauge 13 Fr In distribution
5887150M Catheter Gauge 13 Fr In distribution
5887200G Length 20 cm In distribution
5877300M Catheter Gauge 13 Fr In distribution
5877300B Length 30 cm In distribution
5887120B Length 12.5 cm In distribution
5877300G Length 30 cm In distribution
5887240M Length 24 cm In distribution
5887120G Catheter Gauge 13 Fr In distribution
5877150M Length 15 cm In distribution
5877150G Length 15 cm In distribution
5887240G Catheter Gauge 13 Fr In distribution
5877240G Length 24 cm In distribution
5887150G Catheter Gauge 13 Fr In distribution
5877240B Catheter Gauge 13 Fr In distribution
5877200G Length 20 cm In distribution
5877200M Length 20 cm In distribution
5877150B Length 15 cm In distribution
5887150B Length 15 cm In distribution
5877200B Length 20 cm In distribution
5887200M Length 20 cm In distribution
5877240M Catheter Gauge 13 Fr In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Arrow Teleflex Medical LLC 376
Mahurkar Elite Mozarc Medical US LLC 119
DUO-Flow® Medical Components Inc 106
400XL Medical Components Inc 95
DUO-Split® Medical Components Inc 69
Soft-Line® Duo-Flow® Medical Components Inc 58
Mahurkar Mozarc Medical US LLC 48
Disposable Hemodialysis Access Catheter Set Guangdong Baihe Medical Technology Co., Ltd. 38
Disposable Hemodialysis Access Catheter Set Double Lumen14F*16cm(Straight) Guangdong Baihe Medical Technology Co., Ltd. 31
Turbo-Flo HD Cook Incorporated 28
Niagara catheter Bard Access Systems, Inc. 23
Niagara Slim-Cath catheter Bard Access Systems, Inc. 21

Showing 12 of 59. All products under Catheter, Hemodialysis, Non-Implanted

Recalls

The FDA has not published a severity grade for these. 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 Closed
2026-08-10 Not classified Material/Component Contamination this is a downstream recall of class I recall RES 98777 149521
2026-08-10 Not classified Material/Component Contamination this is a downstream recall of class I recall RES 98777 22,980
2007-08-10 Not classified Other Metal guidewires used in Hemodialysis Catheters may have been reverse loaded within the dispenser. Potential exists for the stiff end of the guidewire to be inserted into the patient instead of the flexible end. 7225 units 2008-04-25

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