400XL

8F X 20CM Subclavian Catheter With Removable "Y" Adaptor

Registry build 21.09.26
1manufacturer
95catalogue 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
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 2024-07-04
Record revised 2024-07-08 (version 5)

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

Catalogue Numbers

Catalogue numbers for 400XL
Catalogue number Size Status
DFXL148IJMB In distribution
DFXL146CES In distribution
DFXL148MB In distribution
DFXL146CEMB In distribution
DFXL144IJCW In distribution
DFXL149MB In distribution
DFXL146MB In distribution
DFXL149CES In distribution
DFXL148CEMB In distribution
DFXL148NEG In distribution
DFXL146NEG In distribution
DDFXL146IJS In distribution
DFXL149NEG In distribution
DDFXL144IJS In distribution
DFXL146IJMB In distribution
DDFXL148IJS In distribution
DFXL144IJ Withdrawn
DFXL146MB Withdrawn
DFXL146MB Withdrawn
MCY308PS Withdrawn
DFXL148CES Withdrawn
DFXL146MT Withdrawn
DFXL146IJCW Withdrawn
DFXL146IJC Withdrawn
DFXL149CT Withdrawn
DFXL148CEMB Withdrawn
RMS26415 Withdrawn
DFXL144IJS Withdrawn
DFXL149 Withdrawn
DFXL144MT Withdrawn
DFXL146IJMB Withdrawn
DFXL149IJMB Withdrawn
DFXL149MB Withdrawn
DFXL148CT Withdrawn
DFXL149IJMB Withdrawn
DFXL149CEMB Withdrawn
DFXL149IJMB Withdrawn
DFXL144CEE Withdrawn
DFXL148MT Withdrawn
DFXL149IJ Withdrawn
RMS26412 Withdrawn
RMS26413 Withdrawn
DFXL146CE Withdrawn
DFXL146IJMB Withdrawn
DFXL148MB Withdrawn
DFXL148NEG Withdrawn
DFXL149NEG Withdrawn
DFXL149CEMB Withdrawn
DFXL148CET Withdrawn
DFXL149CEE Withdrawn
DFXL144IJ Withdrawn
DFXL149MB Withdrawn
RMS26414 Withdrawn
DFXL149IJC Withdrawn
DFXL146CEE Withdrawn
RMS26407 Withdrawn
DFXL146IJS Withdrawn
DFXL148CEMB Withdrawn
DFXL144IJ Withdrawn
RMS26402 Withdrawn
RMS26403 Withdrawn
DFXL148MB Withdrawn
DFXL146 Withdrawn
MCY306PS Withdrawn
AAC26415 Withdrawn
DFXL149MT Withdrawn
DFXL146CET Withdrawn
DFXL149CEMB Withdrawn
DFXL146NEG Withdrawn
DFXL148IJS Withdrawn
DFXL148IJMB Withdrawn
DFXL149CET Withdrawn
RMS03207 Withdrawn
AAC26407 Withdrawn
DFXL146IJ Withdrawn
DFXL146CT Withdrawn
AAC26411 Withdrawn
DFXL146NEG Withdrawn
DFXL144CT Withdrawn
DFXL148IJ Withdrawn
MCDLT118IJ-2 Withdrawn
DFXL148NEG Withdrawn
DFXL149IJS Withdrawn
DFXL149NEG Withdrawn
DFXL148CEE Withdrawn
DFXL148IJC Withdrawn
RMS26411 Withdrawn
AAC26414 Withdrawn
DFXL148IJCW Withdrawn
DFXL146CEMB Withdrawn
DFXL144IJS Withdrawn
DFXL148 Withdrawn
DFXL146CEMB Withdrawn
DFXL148IJMB Withdrawn
DFXL149CE 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
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

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