A sterile valve that is typically a component of an intravenous (IV) administration set and designed to be manually-operated by healthcare staff to regulate the flow of intravenous solution delivered to a patient. This is a single-use device.
| Company | Devices | Share |
|---|---|---|
| Icu Medical, Inc. | 51 | 36% |
| Codan Us Corporation | 17 | 12% |
| Argon Medical Devices, Inc. | 14 | 10% |
| Baxter International Inc. | 13 | 9% |
| Baxter Healthcare Corporation | 8 | 6% |
| Bd Switzerland Sàrl | 7 | 5% |
| Argon Critical Care Systems Singapore Pte. Ltd. | 6 | 4% |
| B. Braun Medical Inc. | 5 | 4% |
| Vygon | 4 | 3% |
| Vygon Corporation | 3 | 2% |
| Safeguard Us Operating, Llc | 2 | 1% |
| Utah Medical Products, Inc. | 2 | 1% |
Company = labeler of record on GUDID. 21 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 |
|---|---|---|
| FMG | Stopcock, i.V. Set | 71 |
| FPA | Set, administration, intravascular | 38 |
| FPA | Set, Administration, Intravascular | 18 |
| DTL | Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass | 17 |
| DXN | System, Measurement, Blood-Pressure, Non-Invasive | 6 |
| DTL | Adaptor, stopcock, manifold, fitting, cardiopulmonary bypass | 4 |
Use these as the dimensions to specify in a tender line.
141 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Intravenous line stopcock", from 21 companies. The largest labeler is Icu Medical, Inc. with 36% of records.
FMG (Stopcock, i.V. Set), FPA (Set, administration, intravascular), FPA (Set, Administration, Intravascular), DTL (Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass)
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.