A short, thin tube intended to be inserted into a peripheral vein (typically on the hand/arm) to enable short-term (< 30 days) intravenous (IV) access for administration of fluids/medication and blood sampling. Also referred to as a peripheral IV catheter, it
| Company | Devices | Share |
|---|---|---|
| Becton, Dickinson And Company | 290 | 31% |
| Navilyst Medical, Inc. | 246 | 26% |
| Delta Med Spa | 98 | 10% |
| Medline Industries, Inc. | 55 | 6% |
| Teleflex Incorporated | 51 | 5% |
| Mckesson Medical-Surgical Inc. | 43 | 5% |
| Togo Medikit Co.,Ltd. | 30 | 3% |
| Terumo Medical Products (Hangzhou) Co., Ltd. | 21 | 2% |
| Terumo Corporation | 18 | 2% |
| Shinva Ande Healthcare Apparatus Co., Ltd | 14 | 1% |
| Terumo (Philippines) Corporation | 13 | 1% |
| Retractable Technologies, Inc. | 12 | 1% |
Company = labeler of record on GUDID. 27 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 3 | 317 |
| FOZ | Catheter, Intravascular, Therapeutic, Short-Term Less Than 3 | 197 |
| FOZ | Catheter,intravascular,therapeutic,short-term less than 30 d | 191 |
| FOZ | Catheter,Intravascular,Therapeutic,Short-Term Less Than 30 D | 20 |
| FPA | Set, administration, intravascular | 17 |
| FGY | Cannula, Injection | 10 |
Use these as the dimensions to specify in a tender line.
948 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Peripheral intravenous cannula", from 27 companies. The largest labeler is Becton, Dickinson And Company with 31% of records.
FOZ (Catheter, intravascular, therapeutic, short-term less than 3), FOZ (Catheter, Intravascular, Therapeutic, Short-Term Less Than 3), FOZ (Catheter,intravascular,therapeutic,short-term less than 30 d), FOZ (Catheter,Intravascular,Therapeutic,Short-Term Less Than 30 D)
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.