DUO-Split®

13F X 20CM DUO-Split® IJ Catheterij Catheter (With 2 Stylets)(With 2 Stylets)

Registry build 21.09.26
1manufacturer
69catalogue numbers in this listing
6510(k) clearances naming this product code
11recalls 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 DUO-Split®
Listed by Medical Components Inc, United States
FDA product code MPB
Device type Catheter, Hemodialysis, Non-Implanted
Device class Class 2
Regulation 21 CFR 876.5540
Establishment Contract manufacturer, Reprocessor, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2019-07-02
Record revised 2021-02-05 (version 6)

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
Packaging Box of 5, box of 10
Distribution end date 2026-04-23

Catalogue Numbers

Catalogue numbers for DUO-Split®
Catalogue number Size Status
DDSP138PS In distribution
DSP139T In distribution
DSP130T In distribution
DDSP136IJS In distribution
DDSP139S In distribution
DSP136T In distribution
DDSP139IJS In distribution
DSP138T In distribution
DSP134IJT In distribution
DDSP139IJS In distribution
DDSP138IJS In distribution
DDSP136IJS In distribution
DDSP134IJS In distribution
DSP139PT In distribution
DDSP139PS In distribution
DSP134PT In distribution
DSP139IJT In distribution
DDSP138IJS In distribution
DSP136PT In distribution
DSP136IJT In distribution
DSP138PT In distribution
DDSP134IJS In distribution
DDSP136S In distribution
DSP138IJT In distribution
DSP139T In distribution
DSP138IJT In distribution
DSP139IJT In distribution
DSP136T In distribution
DSP130T In distribution
DSP134IJT In distribution
DSP138T In distribution
DDSP138S In distribution
DDSP130S In distribution
DDSP136PS In distribution
DSP136IJT In distribution
DDSP138IJC Withdrawn
DSP130S Withdrawn
DSP138PC Withdrawn
DSP134PS Withdrawn
DSP139PT Withdrawn
DSP136IJC Withdrawn
DSP134IJS Withdrawn
DSP138PT Withdrawn
DSP130C Withdrawn
DSP139PC Withdrawn
DSP134S Withdrawn
DDSP139IJC Withdrawn
DDSP136IJC Withdrawn
DSP138C Withdrawn
DSP136PT Withdrawn
DSP138PS Withdrawn
DSP136PC Withdrawn
DSP134PC Withdrawn
DSP139S Withdrawn
DSP136S Withdrawn
DSP139PS Withdrawn
DSP136C Withdrawn
DSP139IJS Withdrawn
DSP139IJC Withdrawn
DSP138IJC Withdrawn
DSP139C Withdrawn
DSP136IJS Withdrawn
DSP138S Withdrawn
DSP134IJC Withdrawn
DSP134C Withdrawn
DSP136PS Withdrawn
DDSP134S Withdrawn
DSP134PT Withdrawn
DSP138IJS Withdrawn

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
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
Duoglide Bard Access Systems, Inc. 24
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

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K250836 2025-08-12
K991320 1999-11-10
K980438 1999-06-10
K983511 1999-06-08
K974236 1999-04-15
K923691 1995-09-25

Recalls

11 of these are 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 Closed
2018-07-12 Class II Process control The suture wings have the potential to crack or break. Potential patient injury includes catheter dislocation, bleeding, and air emboli. The firm has received six complaints (29 broken suture wings) to date for malfunction, without serious 2020-07-02
2018-07-12 Class II Process control The suture wings have the potential to crack or break. Potential patient injury includes catheter dislocation, bleeding, and air emboli. The firm has received six complaints (29 broken suture wings) to date for malfunction, without serious 2020-07-02
2018-07-12 Class II Process control The suture wings have the potential to crack or break. Potential patient injury includes catheter dislocation, bleeding, and air emboli. The firm has received six complaints (29 broken suture wings) to date for malfunction, without serious 2020-07-02
2018-07-12 Class II Process control The suture wings have the potential to crack or break. Potential patient injury includes catheter dislocation, bleeding, and air emboli. The firm has received six complaints (29 broken suture wings) to date for malfunction, without serious 2020-07-02
2018-07-12 Class II Process control The suture wings have the potential to crack or break. Potential patient injury includes catheter dislocation, bleeding, and air emboli. The firm has received six complaints (29 broken suture wings) to date for malfunction, without serious 2020-07-02
2018-07-12 Class II Process control The suture wings have the potential to crack or break. Potential patient injury includes catheter dislocation, bleeding, and air emboli. The firm has received six complaints (29 broken suture wings) to date for malfunction, without serious 2020-07-02
2018-07-12 Class II Process control The suture wings have the potential to crack or break. Potential patient injury includes catheter dislocation, bleeding, and air emboli. The firm has received six complaints (29 broken suture wings) to date for malfunction, without serious 2020-07-02
2018-07-12 Class II Process control The suture wings have the potential to crack or break. Potential patient injury includes catheter dislocation, bleeding, and air emboli. The firm has received six complaints (29 broken suture wings) to date for malfunction, without serious 2020-07-02
2018-07-12 Class II Process control The suture wings have the potential to crack or break. Potential patient injury includes catheter dislocation, bleeding, and air emboli. The firm has received six complaints (29 broken suture wings) to date for malfunction, without serious 2020-07-02
2018-07-12 Class II Process control The suture wings have the potential to crack or break. Potential patient injury includes catheter dislocation, bleeding, and air emboli. The firm has received six complaints (29 broken suture wings) to date for malfunction, without serious 2020-07-02
2018-07-12 Class II Process control The suture wings have the potential to crack or break. Potential patient injury includes catheter dislocation, bleeding, and air emboli. The firm has received six complaints (29 broken suture wings) to date for malfunction, without serious 2020-07-02

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