Consulting Wallah › Device Explorer › Catheters & tubes › Centrally-inserted central venous catheter
Device Explorer · FDA GUDID · GMDN 10729

Centrally-inserted central venous catheter

A flexible tube intended to be introduced into a neck or thoracic vein and often advanced into the superior vena cava for various infusion/aspiration procedures (i.e., non-dedicated) including the intravenous administration of nutrients, fluids, chemotherapeut

US‑registered devices2,718in commercial distribution
Companies8labelers on GUDID
Single‑use100%of device records
Sterile98%labelled sterile
Prescription97%Rx‑only share
ImplantableYesGMDN flag
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Share of device records

Teleflex Incorporated2,29384%
Cook Incorporated2098%
Bard Access Systems, Inc.683%
Vygon Corporation602%
Medical Components, Inc.512%
Guangdong Baihe Medical Technology Co., Ltd.130%
Vygon-Erzeugnisse Für Medizin Und Chirurgie-Gmbh Und Co. Kg120%
Icu Medical, Inc.120%

Top labelers

CompanyDevicesShare
Teleflex Incorporated2,29384%
Cook Incorporated2098%
Bard Access Systems, Inc.683%
Vygon Corporation602%
Medical Components, Inc.512%
Guangdong Baihe Medical Technology Co., Ltd.130%
Vygon-Erzeugnisse Für Medizin Und Chirurgie-Gmbh Und Co. Kg120%
Icu Medical, Inc.120%

Company = labeler of record on GUDID. 8 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Able Central Venous Catheter Triple Lumen 7F*30cAble Central Venous Catheter Triple Lumen 7F*20cAble Central Venous Catheter Double Lumen 7F*16cAble Central Venous Catheter Double Lumen 4F*12.Able Central Venous Catheter Single Lumen 16G*8cAble Central Venous Catheter Double Lumen 7F*30cAble Central Venous Catheter Double Lumen 7F*20cAble Central Venous Catheter Single Lumen 14G*22Able Central Venous Catheter Triple Lumen 7F*16cAble Central Venous Catheter Double Lumen 8F*05cAble Central Venous Catheter Single Lumen 14G*16Able Central Venous Catheter Single Lumen 18G*25VYGONICU MedicalPRO-LINE CT PRESSURE INJECTABLE CVC (ISOPLAST) (Pro-Line® CT

Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.

FDA product codes

CodeNameDevices
FOZCatheter,intravascular,therapeutic,short-term less than 30 d1,162
DQYCATHETER, PERCUTANEOUS598
DQYCatheter, percutaneous389
FOZCatheter, intravascular, therapeutic, short-term less than 3310
LJSCatheter,intravascular,therapeutic,long-term greater than 30195
LJSCatheter, intravascular, therapeutic, long-term greater than116

GMDN & GCC registration

  • GMDN code 10729 · implantable
  • Single‑use 100% · sterile 98% · Rx‑only 97% · OTC 0%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Catheter Gauge (French) · 111Length (Centimeter) · 76Length (Inch) · 5Catheter Length (Centimeter) · 2Catheter Length (Inch) · 1

Use these as the dimensions to specify in a tender line.

How many centrally-inserted central venous catheter products are registered in the US?

2,718 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Centrally-inserted central venous catheter", from 8 companies. The largest labeler is Teleflex Incorporated with 84% of records.

Which FDA product codes apply?

FOZ (Catheter,intravascular,therapeutic,short-term less than 30 d), DQY (CATHETER, PERCUTANEOUS), DQY (Catheter, percutaneous), FOZ (Catheter, intravascular, therapeutic, short-term less than 3)

Is this the same as UAE/GCC registration?

No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.

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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.

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