Soft-Line® Duo-Flow®
11.5F X 12CM Raulerson DUO-Flow IJ Double Lumen Catheter SET (10 PER BOX) (KIT HAS 5 YR EXP Date)
1manufacturer
58catalogue numbers in this listing
6510(k) clearances naming this product code
11recalls on this code
Who Else Makes It
Registered in Guangdong.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Guangdong Baihe Medical Technology Co., Ltd. | Foshan | Guangdong | Contract manufacturer | 4 |
Record
| 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 |
| Premarket notification | Exempt |
| Record published | 2024-05-11 |
| Record revised | 2024-08-08 (version 6) |
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 | 2026-04-29 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| T73M | In distribution | |
| DT74M | In distribution | |
| DT96M | In distribution | |
| T4000 | In distribution | |
| DT73M | In distribution | |
| T4400 | In distribution | |
| T96M | In distribution | |
| DT116M | In distribution | |
| T3500 | In distribution | |
| T4000 | In distribution | |
| DT114M | In distribution | |
| DT94M | In distribution | |
| DT98M | In distribution | |
| T4400 | In distribution | |
| T3500 | In distribution | |
| DT118M | In distribution | |
| T118IJ-2 | Withdrawn | |
| T114IJ-2 | Withdrawn | |
| DT118IJC-2 | Withdrawn | |
| XTP116IJS-1 | Withdrawn | |
| DT119C | Withdrawn | |
| T94M | Withdrawn | |
| T96C | Withdrawn | |
| DT94C | Withdrawn | |
| T119C | Withdrawn | |
| XTP114IJSE | Withdrawn | |
| T94C | Withdrawn | |
| T116IJ-2 | Withdrawn | |
| T98M | Withdrawn | |
| T73M | Withdrawn | |
| T116IJS-2 | Withdrawn | |
| T116IJS-2E. | Withdrawn | |
| T118C | Withdrawn | |
| T114IJ-2 | Withdrawn | |
| T116M | Withdrawn | |
| T114C | Withdrawn | |
| T118IJS-2E. | Withdrawn | |
| T114M | Withdrawn | |
| T116IJ-2 | Withdrawn | |
| DT114C | Withdrawn | |
| T114IJS-2 | Withdrawn | |
| DT96C | Withdrawn | |
| T116C | Withdrawn | |
| DT118C | Withdrawn | |
| T74M | Withdrawn | |
| T118M | Withdrawn | |
| T118IJS-2 | Withdrawn | |
| DT98C | Withdrawn | |
| XTP116IJSE | Withdrawn | |
| T114IJC-2 | Withdrawn | |
| T116IJC-2 | Withdrawn | |
| T116IJS-2E. | Withdrawn | |
| T96M | Withdrawn | |
| DT116C | Withdrawn | |
| T118IJC-2 | Withdrawn | |
| T94M | Withdrawn | |
| T118IJ-2 | Withdrawn | |
| XTP118IJSE | Withdrawn |
Same 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 |
| 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
| 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.
| 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.