A hand-held cylindrical device designed to be used together with an evacuated blood collection tube to draw blood samples from a patient. It is typically a hollow plastic adaptor into which the blood collection tube is inserted and to which the user attaches a
| Company | Devices | Share |
|---|---|---|
| Icu Medical, Inc. | 12 | 14% |
| Cardinal Health 200, Llc | 8 | 10% |
| Kb Medical (Group), Inc. | 7 | 8% |
| Itl Asia Pacific Sdn. Bhd. | 7 | 8% |
| Gcb Medical Llc | 4 | 5% |
| Dynarex Corporation | 4 | 5% |
| Globe Scientific Inc. | 4 | 5% |
| Medline Industries, Inc. | 4 | 5% |
| Aeon Biotherapeutics Corp. | 3 | 4% |
| Sarstedt Aktiengesellschaft & Co.Kg | 3 | 4% |
| Velano Vascular, Inc. | 3 | 4% |
| Sol-Millennium Medical, Inc. | 3 | 4% |
Company = labeler of record on GUDID. 24 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 |
|---|---|---|
| JKA | Tubes, Vials, Systems, Serum Separators, Blood Collection | 24 |
| KST | System, Blood Collection, Vacuum-Assisted, Manual | 19 |
| JKA | Tubes, vials, systems, serum separators, blood collection | 19 |
| FMI | Needle, Hypodermic, Single Lumen | 11 |
| KST | System, blood collection, vacuum-assisted, manual | 7 |
| LXG | Equipment, Laboratory, General Purpose, Labeled Or Promoted | 5 |
Use these as the dimensions to specify in a tender line.
No closely related category with 50+ devices.
83 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Blood collection tube holder, single-use", from 24 companies. The largest labeler is Icu Medical, Inc. with 14% of records.
JKA (Tubes, Vials, Systems, Serum Separators, Blood Collection), KST (System, Blood Collection, Vacuum-Assisted, Manual), 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.