A small, stand-alone, Luer-activated needleless plastic valve intended to mate two related intravenous (IV) line devices [e.g., hypodermic syringe and catheter port or tubing from an IV administration set] and hold them in a secured, sealed, locked position un
| Company | Devices | Share |
|---|---|---|
| Icu Medical, Inc. | 169 | 69% |
| Rymed Technologies, Llc | 41 | 17% |
| Asset Medikal Tasarim Sanayi Ve Ticaret Anonim Sirketi | 13 | 5% |
| Nexus Medical, Llc | 8 | 3% |
| Vygon | 3 | 1% |
| Vygon Corporation | 3 | 1% |
| Bd Switzerland Sàrl | 2 | 1% |
| B. Braun Medical Inc. | 1 | 0% |
| Yukon Medical, Llc | 1 | 0% |
| Mps Medical, Inc | 1 | 0% |
| Quest Medical Inc | 1 | 0% |
| Cair Lgl | 1 | 0% |
Company = labeler of record on GUDID. 13 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 | 98 |
| FPA | Set, Administration, Intravascular | 66 |
| ONB | Closed antineoplastic and hazardous drug reconstitution and | 62 |
| FMG | Stopcock, i.V. Set | 10 |
| FOZ | Catheter, intravascular, therapeutic, short-term less than 3 | 3 |
| FOZ | Catheter,intravascular,therapeutic,short-term less than 30 d | 3 |
Use these as the dimensions to specify in a tender line.
245 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Neutral-pressure intravenous line needleless valve-connector", from 13 companies. The largest labeler is Icu Medical, Inc. with 69% of records.
FPA (Set, administration, intravascular), FPA (Set, Administration, Intravascular), ONB (Closed antineoplastic and hazardous drug reconstitution and ), FMG (Stopcock, i.V. Set)
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.