A sterile, hand-held cylindrical device with a pre-attached needle 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 with a pre-attached blood collection needle a
| Company | Devices | Share |
|---|---|---|
| Myco Medical Supplies Inc. | 13 | 18% |
| Guangzhou Improve Medical Instruments Co., Ltd. | 12 | 17% |
| Jiangsu Micsafe Medical Tehcnology Co.,Ltd. | 12 | 17% |
| Medivena, Llc | 7 | 10% |
| Jiangsu Caina Medical Co.,Ltd | 4 | 6% |
| Greiner Bio-One Gmbh | 4 | 6% |
| Itl Asia Pacific Sdn. Bhd. | 3 | 4% |
| Innovative Medical Technologies, Inc. | 2 | 3% |
| Resilient Medical Solutions, Llc | 2 | 3% |
| Prestige Ameritech, Ltd. | 2 | 3% |
| Retractable Technologies, Inc. | 2 | 3% |
| Transparent Supply Solutions Ltd. | 2 | 3% |
Company = labeler of record on GUDID. 17 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 | 43 |
| FMI | Needle, Hypodermic, Single Lumen | 33 |
| FMI | Needle, hypodermic, single lumen | 9 |
| KST | System, Blood Collection, Vacuum-Assisted, Manual | 5 |
| JKA | Tubes, vials, systems, serum separators, blood collection | 3 |
| FMH | Container, Specimen, Sterile | 2 |
Use these as the dimensions to specify in a tender line.
No closely related category with 50+ devices.
72 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Blood collection tube holder/needle", from 17 companies. The largest labeler is Myco Medical Supplies Inc. with 18% of records.
JKA (Tubes, Vials, Systems, Serum Separators, Blood Collection), FMI (Needle, Hypodermic, Single Lumen), FMI (Needle, hypodermic, single lumen), KST (System, Blood Collection, Vacuum-Assisted, Manual)
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.