Medline

NO-Cath Radial Arterial Premium KIT

Registry build 21.09.26
1manufacturer
24catalogue numbers in this listing

Who Else Makes It

Registered in Zhejiang.

Chinese manufacturers registered for FDA product code CBT
Manufacturer City Province Registered as Device types
Hantech Medical Device Co., Ltd. Cixi Zhejiang Contract manufacturer 18

Record

Regulatory record for Medline
Listed by Medline Industries, Inc., United States
FDA product code CBT
Device type Arterial Blood Sampling Kit
Device class Class 1
Regulation 21 CFR 868.1100
Premarket notification Exempt
Record published 2020-05-04
Record revised 2025-11-20 (version 4)

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 Case of 5, case of 20, case of 10, case of 25
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Medline
Catalogue number Size Status
ART995 In distribution
ARTNC110 In distribution
ARTNC115 In distribution
ART1120 In distribution
ARTNC135 In distribution
ARTNC110 In distribution
ART1110A In distribution
ART1070A In distribution
ARTNC221 In distribution
ARTNC115 In distribution
ART775B In distribution
DYNDC3235C In distribution
ART1110B In distribution
ART1180 In distribution
DYNDC2707A In distribution
ART1070 In distribution
ART1145 In distribution
DYNDA1453A In distribution
ART1160 In distribution
ART1175 In distribution
ART1160 In distribution
ART1010B In distribution
ART890A In distribution
ART1110 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Pulset Westmed, Inc. 49
Centurion Centurion Medical Products Corporation 22
Medex ICU Medical, Inc 22
Regard™ Resource Optimization & Innovation, L.L.C. 16
AirLife™ Airlife, Inc. 16
Deltran Utah Medical Products, Inc. 14
A-Line Westmed, Inc. 12
Pulset SunMed Group Holdings, LLC 11
Atellica® VTR Syringes SunMed Group Holdings, LLC 7
Blood Gas Sampler Westmed, Inc. 7
Atellica® VTR Syringes Westmed, Inc. 5
Arterial Blood Sampling Kit Utah Medical Products, Inc. 4

Showing 12 of 41. All products under Arterial Blood Sampling Kit

Recalls Naming This Product

6 recalls name this product by its own identifiers, the UDI on its label.

Recalls naming the identifiers of Medline
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Medline Industries, LP – Northfield UDI-DI 2026-05-21 Class II Nonconforming Material/Component The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing in 5,698 kits
Medline Industries, LP – Northfield UDI-DI 2026-05-21 Class II Nonconforming Material/Component The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing in 48075 kits
Medline Industries, LP – Northfield UDI-DI 2023-11-15 Class I Nonconforming Material/Component Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride Irrigation USP, Sterile Water for Irrigation USP and Saline Flush Syringe. Nurse As
Medline Industries, LP – Northfield UDI-DI 2023-05-18 Class II Device Design Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams. 269985 units
Medline Industries, LP – Northfield UDI-DI 2023-05-18 Class II Device Design Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams. # included in 3,740,814 units total
Medline Industries, LP – Northfield UDI-DI 2023-05-18 Class II Device Design Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams. 2590 units

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