Consulting Wallah › Device Explorer › Catheters & tubes › Vascular guide-catheter, single-use
Device Explorer · FDA GUDID · GMDN 17846

Vascular guide-catheter, single-use

A flexible tube intended to be used for the percutaneous transluminal passage and placement of a diagnostic/interventional catheter, lead (e.g., pacing lead, balloon dilatation catheter), needle or guidewire through its lumen(s), within the vascular system. It

US‑registered devices9,177in commercial distribution
Companies77labelers on GUDID
Single‑use100%of device records
Sterile100%labelled sterile
Prescription100%Rx‑only share
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Share of device records

Medtronic, Inc.4,29647%
Boston Scientific Corporation1,22813%
Cordis Corporation8109%
Pendracare International B.V.5446%
Oscor Inc.4305%
Cordis Us Corp.3123%
Centerpoint Systems Llc1602%
Asahi Intecc Co., Ltd.1552%

Top labelers

CompanyDevicesShare
Medtronic, Inc.4,29647%
Boston Scientific Corporation1,22813%
Cordis Corporation8109%
Pendracare International B.V.5446%
Oscor Inc.4305%
Cordis Us Corp.3123%
Centerpoint Systems Llc1602%
Asahi Intecc Co., Ltd.1552%
St. Jude Medical, Inc.1151%
Terumo Corporation871%
Cerenovus, Inc.851%
Micro Therapeutics, Inc.771%

Company = labeler of record on GUDID. 77 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Broadway SystemBroadway 8EchoAXS LiftAXS VECTA 46Stroke Fast PackAXS INFINITY LS PLUSAXS Catalyst 7AXS OffsetDAC 044DAC 070DAC 057DAC 038AXS INFINITY LSAXS Catalyst 6AXS Catalyst 5

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

FDA product codes

CodeNameDevices
DQYCATHETER, PERCUTANEOUS8,618
DQYCatheter, percutaneous2,623
DQYCatheter, Percutaneous1,205
DYBINTRODUCER, CATHETER439
DYBIntroducer, Catheter325
DQOCATHETER, INTRAVASCULAR, DIAGNOSTIC196

GMDN & GCC registration

  • GMDN code 17846 · 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

Length (Centimeter) · 8,446Catheter Gauge (French) · 8,173Catheter Length (Centimeter) · 824Lumen/Inner Diameter (Millimeter) · 490Outer Diameter (Millimeter) · 445Lumen/Inner Diameter (Inch) · 241

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

How many vascular guide-catheter, single-use products are registered in the US?

9,177 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Vascular guide-catheter, single-use", from 77 companies. The largest labeler is Medtronic, Inc. with 47% of records.

Which FDA product codes apply?

DQY (CATHETER, PERCUTANEOUS), DQY (Catheter, percutaneous), DQY (Catheter, Percutaneous), DYB (INTRODUCER, CATHETER)

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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