Argyle

Acute Single Lumen Catheter Kit,Curved Extension,8 Fr/Ch (2.7 mm) x 15 cm

Registry build 21.09.26
1manufacturer
2catalogue numbers in this listing
1recall

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 Argyle
Listed by Mozarc Medical US LLC, United States
FDA product code MPB
Device type Catheter, Hemodialysis, Non-Implanted
Device class Class 2
Regulation 21 CFR 876.5540
Establishment Specification developer, Manufacturer
510(k) K896252
Record published 2015-08-30
Record revised 2025-04-29 (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
Label carries lot or batch number, expiry date
Packaging Pack_or_inner_pack of 5
Sizes Length 15 cm; catheter gauge 8 Fr
Distribution end date 2020-11-25

Catalogue Numbers

Catalogue numbers for Argyle
Catalogue number Size Status
8817232018 Catheter Gauge 8 Fr In distribution
8831173012 Length 15 cm Withdrawn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

Recalls

1 of these is 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 Quantity
2026-04-29 Class II Under Investigation by firm The Tegaderm CHG dressing, as specified in product labeling, was missing from certain lots of Mahurkar Elite PASS Trays. 25627

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