DUO-Flow®

11.5F X 15CM RAULERSON PRE-CURVED Duo-Flow® IJ DOUBLE LUMEN CATHETER WITH SOFT TIP SET

Registry build 21.09.26
1manufacturer
106catalogue 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-Flow®
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 2019-07-12
Record revised 2023-04-14 (version 7)

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

Catalogue Numbers

Catalogue numbers for DUO-Flow®
Catalogue number Size Status
DXTP94IJS In distribution
AS0912241 In distribution
MCDLT116IJ In distribution
AC0912151 In distribution
AS0911241 In distribution
DXTP98IJS In distribution
DXTP116IJC-2 In distribution
AS099201 In distribution
DXTP118IJC In distribution
AS099201 In distribution
MCDLT118IJ-2 In distribution
AC0911121 In distribution
MCDLT114IJS In distribution
AS099151 In distribution
AS0911121 In distribution
AC0911201 In distribution
AC0911151 In distribution
AS099101 In distribution
DXTP118IJS In distribution
DXTP116IJS-2 In distribution
AC099121 In distribution
AS0911151 In distribution
AC0912201 In distribution
AC0912131 In distribution
AC0911121 In distribution
DXTP118IJS-2 In distribution
AC0911151 In distribution
AS0912201 In distribution
AC099751 In distribution
DXTP116IJC In distribution
DXTP114IJS In distribution
AC0911101 In distribution
AC099751 In distribution
DXTP96IJS In distribution
MCDLT114IJ-2 In distribution
AS0911241 In distribution
AC0911101 In distribution
AS099121 In distribution
AS0912201 In distribution
DXTP118IJC-2 In distribution
AS0911201 In distribution
AC0911201 In distribution
AC099121 In distribution
AC099151 In distribution
AS0912151 In distribution
AS0911121 In distribution
AS0911151 In distribution
XTP118MTE In distribution
AS099151 In distribution
AS0912241 In distribution
DXTP114IJC-2 In distribution
MCDLT114IJ In distribution
AS099101 In distribution
MCDLT118IJ-2S In distribution
XTP116MTE In distribution
AC0912151 In distribution
AC099151 In distribution
DXTP114IJC In distribution
AC0912131 In distribution
DXTP114IJS-2 In distribution
AS099121 In distribution
AS0912151 In distribution
DXTP116IJS In distribution
MCDLT116IJ-2 In distribution
AS0911201 In distribution
AC0912201 In distribution
MCDLT118IJ In distribution
DFXL148CE Withdrawn
TRAY #415 Withdrawn
MCDLT118IJ Withdrawn
DFXL144IJC Withdrawn
XTP116IJS Withdrawn
TRAY #414 Withdrawn
XTP96IJC Withdrawn
XTP114IJC-2 Withdrawn
MCDLT114IJ Withdrawn
XTP118IJS Withdrawn
DXTP96IJC Withdrawn
MCDLT114IJ-2 Withdrawn
XTP118IJC-2 Withdrawn
XTP94IJS Withdrawn
TRAY #332 Withdrawn
DDSP134PS Withdrawn
XTP118IJS-2 Withdrawn
MCDLT114IJ Withdrawn
DXTP98IJC Withdrawn
XTP118IJC Withdrawn
XTP116IJC-2 Withdrawn
XTP98IJC Withdrawn
MCDLT116IJ-2 Withdrawn
XTP116IJS-2 Withdrawn
DXTP94IJC Withdrawn
XTP114IJS Withdrawn
MCDLT116IJ Withdrawn
XTP116IJC Withdrawn
XTP94IJC Withdrawn
XTP98IJS Withdrawn
MCDLT114IJ-2 Withdrawn
DXTP116IJS-1 Withdrawn
XTP114IJS-2 Withdrawn
MCDLT118IJ Withdrawn
XTP96IJS Withdrawn
XTP114IJC Withdrawn
MCDLT116IJ-2 Withdrawn
MCDLT116IJ Withdrawn
MCDLT118IJ-2 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
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
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

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2,581device types they are registered for
340,248device records, each naming its maker
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