A short, thin tube intended for short-term (<= 30 days) percutaneous access to a peripheral artery for invasive blood pressure monitoring and arterial blood sampling; it may in addition be intended for peripheral intravenous (IV) or subcutaneous use for blood
| Company | Devices | Share |
|---|---|---|
| Teleflex Incorporated | 404 | 86% |
| Cook Incorporated | 54 | 12% |
| Becton, Dickinson And Company | 4 | 1% |
| Argon Critical Care Systems Singapore Pte. Ltd. | 4 | 1% |
| Vygon | 2 | 0% |
Company = labeler of record on GUDID. 5 companies in total; top 12 shown. Click headers to sort.
Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.
| Code | Name | Devices |
|---|---|---|
| DQX | Wire, guide, catheter | 161 |
| DQX | WIRE, GUIDE, CATHETER | 127 |
| DQY | Catheter, percutaneous | 127 |
| DQO | CATHETER, INTRAVASCULAR, DIAGNOSTIC | 36 |
| DQY | CATHETER, PERCUTANEOUS | 28 |
| FOZ | Catheter, intravascular, therapeutic, short-term less than 3 | 6 |
Use these as the dimensions to specify in a tender line.
468 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Peripheral artery cannula", from 5 companies. The largest labeler is Teleflex Incorporated with 86% of records.
DQX (Wire, guide, catheter), DQX (WIRE, GUIDE, CATHETER), DQY (Catheter, percutaneous), DQO (CATHETER, INTRAVASCULAR, DIAGNOSTIC)
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.