Consulting Wallah › Device Explorer › Catheters & tubes › Arterial blood pressure catheter
Device Explorer · FDA GUDID · GMDN 10689

Arterial blood pressure catheter

A sterile, thin flexible tube intended for short-term (<= 30 days) percutaneous placement within an artery for continuous blood pressure monitoring. It is typically interfaced with a parent device (e.g., external blood pressure transducer) and may be used for

US‑registered devices226in commercial distribution
Companies5labelers on GUDID
Single‑use100%of device records
Sterile100%labelled sterile
Prescription100%Rx‑only share
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Share of device records

Teleflex Incorporated21394%
Valflux Group, Llc63%
Argon Critical Care Systems Singapore Pte. Ltd.42%
Vygon21%
Centurion Medical Products Corporation10%

Top labelers

CompanyDevicesShare
Teleflex Incorporated21394%
Valflux Group, Llc63%
Argon Critical Care Systems Singapore Pte. Ltd.42%
Vygon21%
Centurion Medical Products Corporation10%

Company = labeler of record on GUDID. 5 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

VYGONCAREFLOW(TM) 1 LUMEN 4FR X 200MMCAREFLOW(TM) 1 LUMEN 3FR X 60MMCAREFLOW(TM) 1 LUMEN 3FR X 200MMCAREFLOW(TM) 1 LUMEN 2.5FR X 60MMHIGH PRESSURE TUBINGARROWCenturion

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

FDA product codes

CodeNameDevices
DQXWIRE, GUIDE, CATHETER185
DQXWire, guide, catheter22
DQYCATHETER, PERCUTANEOUS7
DXTINJECTOR AND SYRINGE, ANGIOGRAPHIC6
FOZCatheter,Intravascular,Therapeutic,Short-Term Less Than 30 D4
DQOCATHETER, INTRAVASCULAR, DIAGNOSTIC2

GMDN & GCC registration

  • GMDN code 10689 · non‑implantable
  • Single‑use 100% · sterile 100% · Rx‑only 100% · 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) · 6Length (Centimeter) · 6

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

No closely related category with 50+ devices.

How many arterial blood pressure catheter products are registered in the US?

226 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Arterial blood pressure catheter", from 5 companies. The largest labeler is Teleflex Incorporated with 94% of records.

Which FDA product codes apply?

DQX (WIRE, GUIDE, CATHETER), DQX (Wire, guide, catheter), DQY (CATHETER, PERCUTANEOUS), DXT (INJECTOR AND SYRINGE, ANGIOGRAPHIC)

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.

How do I get quotes?

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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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