An invasive, hollow, tubular, metal device intended to puncture a vein to collect blood and/or for transient (<24 hours) or short-term (<= 30 days) administration of intravenous (IV) fluids. It includes wings for fixation/placement and may include tubing and/o
| Company | Devices | Share |
|---|---|---|
| Icu Medical, Inc. | 39 | 39% |
| Hindustan Syringes And Medical Devices Limited | 16 | 16% |
| Exel International | 12 | 12% |
| Mercedes Medical, Llc | 9 | 9% |
| Mckesson Medical-Surgical Inc. | 8 | 8% |
| Delta Med Spa | 4 | 4% |
| Endure Industries | 3 | 3% |
| Henry Schein, Inc. | 3 | 3% |
| Regen Lab Sa | 3 | 3% |
| Merit Pharmaceutical | 1 | 1% |
| Innovative Medical Technologies, Inc. | 1 | 1% |
Company = labeler of record on GUDID. 11 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 |
|---|---|---|
| FPA | Set, administration, intravascular | 38 |
| FPA | Set, Administration, Intravascular | 27 |
| JKA | Tubes, Vials, Systems, Serum Separators, Blood Collection | 16 |
| FMI | Needle, Hypodermic, Single Lumen | 12 |
| FOZ | Catheter,Intravascular,Therapeutic,Short-Term Less Than 30 D | 6 |
| JKA | Tubes, vials, systems, serum separators, blood collection | 3 |
Use these as the dimensions to specify in a tender line.
99 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Venous butterfly needle/set", from 11 companies. The largest labeler is Icu Medical, Inc. with 39% of records.
FPA (Set, administration, intravascular), FPA (Set, Administration, Intravascular), JKA (Tubes, Vials, Systems, Serum Separators, Blood Collection), FMI (Needle, Hypodermic, Single Lumen)
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.