A sterile, thin, flexible tube intended to be inserted into the peripheral vasculature of a patient to enable short-term (< 30 days) intravascular access; it is not intended to be advanced to the central vasculature. It typically includes dedicated accessories
| Company | Devices | Share |
|---|---|---|
| Delta Med Spa | 95 | 26% |
| Teleflex Incorporated | 55 | 15% |
| Maquet Cardiopulmonary Ag | 45 | 12% |
| Icu Medical, Inc. | 32 | 9% |
| Argon Medical Devices, Inc. | 25 | 7% |
| Access Scientific, Llc | 21 | 6% |
| Nipro Medical Corporation | 21 | 6% |
| Vygon Corporation | 14 | 4% |
| Edwards Lifesciences Llc | 14 | 4% |
| Exel International | 12 | 3% |
| Pfm Medical Incorporated | 11 | 3% |
| Bard Access Systems, Inc. | 7 | 2% |
Company = labeler of record on GUDID. 17 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 |
|---|---|---|
| FOZ | Catheter,Intravascular,Therapeutic,Short-Term Less Than 30 D | 114 |
| FOZ | Catheter,intravascular,therapeutic,short-term less than 30 d | 76 |
| DWF | CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPA | 45 |
| LJS | Catheter,intravascular,therapeutic,long-term greater than 30 | 31 |
| OWL | Peripheral Catheter Insertion Kit | 27 |
| FOZ | Catheter, Intravascular, Therapeutic, Short-Term Less Than 3 | 24 |
Use these as the dimensions to specify in a tender line.
372 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Peripheral vascular catheter", from 17 companies. The largest labeler is Delta Med Spa with 26% of records.
FOZ (Catheter,Intravascular,Therapeutic,Short-Term Less Than 30 D), FOZ (Catheter,intravascular,therapeutic,short-term less than 30 d), DWF (CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPA), LJS (Catheter,intravascular,therapeutic,long-term greater than 30)
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.