A collection of noninvasive devices intended to prepare and/or dress a peripheral vein intravenous (IV) access site. It typically includes devices such as a tourniquet, disinfected swabs, dressings, tape, gauze, and gloves; neither the IV access device nor pha
| Company | Devices | Share |
|---|---|---|
| Centurion Medical Products Corporation | 518 | 32% |
| Medline Industries, Inc. | 372 | 23% |
| Bound Tree Medical, Llc | 155 | 9% |
| Medical Action Industries Inc. | 150 | 9% |
| Haslam Medical, Inc. | 118 | 7% |
| Vygon Corporation | 70 | 4% |
| Cardinal Health 200, Llc | 52 | 3% |
| Owens & Minor Distribution, Inc. | 45 | 3% |
| Stradis Medical, Llc | 40 | 2% |
| Medsource International Llc | 29 | 2% |
| Mckesson Medical-Surgical Inc. | 21 | 1% |
| Becton, Dickinson And Company | 14 | 1% |
Company = labeler of record on GUDID. 26 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 |
|---|---|---|
| LRS | I.V. start kit | 1,519 |
| LRS | I.V. Start Kit | 172 |
| FPA | Set, Administration, Intravascular | 47 |
| FOZ | Catheter,intravascular,therapeutic,short-term less than 30 d | 15 |
| LRP | TRAY, SURGICAL | 15 |
| PEZ | Central venous catheter dressing change kit | 13 |
Use these as the dimensions to specify in a tender line.
1,634 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Peripheral intravenous catheterization support kit", from 26 companies. The largest labeler is Centurion Medical Products Corporation with 32% of records.
LRS (I.V. start kit), LRS (I.V. Start Kit), FPA (Set, Administration, Intravascular), 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.