Ruby Intravascular Catheter

Ruby Intravascular Catheter is a sterile, single-use 20-gauge catheter with a usable length of 1.30 inches. It is intended for short-term vascular access to sample blood, monitor blood…

Registry build 21.09.26

Ruby Intravascular Catheter is a sterile, single-use 20-gauge catheter with a usable length of 1.30 inches. It is intended for short-term vascular access to sample blood, monitor blood pressure or deliver intravenous fluids. It is also suitable for use with power injectors.

A valve in the hub automatically restricts blood flow when the insertion needle is removed, until a secure Luer connection is made. A slider deploys and retracts a catheter-guiding element with an atraumatic tip positioned between the catheter and needle.

Listed Item

The RUBY™ Intravascular Catheter consists of a radiopaque catheter having a usable length of 1.30 inches in 20-gauge size.

Patient Range and Insertion Features

The catheter is indicated for adults and pediatric patients weighing at least 10 kg, with selection considering vascular anatomy, the infused solution and therapy duration. A flashback chamber provides blood-return visualization, and a safety container shields the sharp. The catheter itself is radiopaque.

12manufacturers in China registered for this device type
1catalogue number
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Shandong (3), Guangdong (3), Jiangsu (2). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code FOZ
Manufacturer City Province Registered as Device types
Amsino Medical (Shanghai) Co., Ltd. Shanghai Shanghai Contract manufacturer 22
Bioxin Medical Co., Ltd. Weihai Shandong Contract manufacturer 8
Weihai Jierui Medical Products Co., Ltd. Weihai Shandong Contract manufacturer 3
Becton Dickinson Medical Devices Co., Ltd. Suzhou Suzhou Jiangsu Contract manufacturer 2
Jiangsu NEW Pentastar Medical Products Co., Ltd. Changzhou Jiangsu Exporter 146
Zhejiang Kindly Medical Devices Co., Ltd. Wenzhou Zhejiang Contract manufacturer 16
Terumo Medical Products (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 7
Shandong Ande Healthcare Apparatus Co., Ltd. Zibo Shandong Manufacturer 7
Jiangxi Sanxin Medtec Co., Ltd. Nanchang Jiangxi Manufacturer 6
Haolang Technology (Foshan) Limited Corporation Foshan Guangdong Contract manufacturer 6
Guangdong Baihe Medical Technology Co., Ltd. Foshan Guangdong Contract manufacturer 4
Foshan Special Medical Co., Ltd. Foshan Guangdong Manufacturer 3

Record

Regulatory record for Ruby Intravascular Catheter
Listed by Venocare, Inc., United States
FDA product code FOZ
Device type Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
Device class Class 2
Regulation 21 CFR 880.5200
Establishment Specification developer, Complaint-file establishment, Manufacturer
510(k) K243105
Record published 2026-04-08
Record revised 2026-07-15 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Packaging Pack of 10, pack of 20, pack of 40

Catalogue Numbers

Catalogue numbers for Ruby Intravascular Catheter
Catalogue number Size Status
VNC20130FG In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Arrow Teleflex Medical LLC 2,368
Cook Cook Incorporated 250
Cook Spectrum Cook Incorporated 225
Jelco ICU Medical, Inc 104
Medline Medline Industries, Inc. 95
Deltaven Fast Flash Delta Med SpA 77
Deltaven Delta Med SpA 73
PowerGlide Pro Bard Access Systems, Inc. 63
Peripheral Catheter Insertion Kit Bard Access Systems, Inc. 62
Able Central Venous Catheter Guangdong Baihe Medical Technology Co., Ltd. 62
Curaplex Bound Tree Medical, LLC 61
BD Cathena™ Safety IV Catheter Becton, Dickinson AND Company 59

Showing 12 of 285. All products under Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K260432 2026-09-02
K243105 2025-05-16

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