400XL IJ400XL IJ

14F X 24CM 400XL IJ14F X 24CM 40 Catheter Setcatheter SET

Registry build 21.09.26
1manufacturer
5catalogue 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 400XL IJ400XL IJ
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 2019-07-31
Record revised 2022-05-12 (version 3)

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
Distribution end date 2022-06-20

Catalogue Numbers

Catalogue numbers for 400XL IJ400XL IJ
Catalogue number Size Status
DDFXL149IJS In distribution
DDFXL148IJC Withdrawn
DDFXL146IJC Withdrawn
DDFXL149IJC Withdrawn
DDFXL144IJC Withdrawn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
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

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