A device intended to be used during patient blood collection to facilitate transfer of a clinical blood specimen from blood collection tubing or a needle to a blood specimen receptacle (e.g., evacuated blood collection tube, adapted syringe). It is designed to
| Company | Devices | Share |
|---|---|---|
| Promisemed Medical Devices Inc. | 30 | 49% |
| Greiner Bio-One Gmbh | 7 | 11% |
| Sarstedt Aktiengesellschaft & Co.Kg | 5 | 8% |
| Terumo Medical Products (Hangzhou) Co., Ltd. | 5 | 8% |
| Medivena, Llc | 3 | 5% |
| Becton, Dickinson And Company | 2 | 3% |
| Nsp Tech Pte Ltd | 2 | 3% |
| Fresenius Kabi Ag | 1 | 2% |
| Terumo Corporation | 1 | 2% |
| Nexus Medical, Llc | 1 | 2% |
| Nipro Medical Corporation | 1 | 2% |
| Icu Medical, Inc. | 1 | 2% |
Company = labeler of record on GUDID. 14 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 |
|---|---|---|
| FMI | Needle, Hypodermic, Single Lumen | 34 |
| JKA | Tubes, Vials, Systems, Serum Separators, Blood Collection | 7 |
| FPA | Set, Administration, Intravascular | 6 |
| FMI | Needle, hypodermic, single lumen | 6 |
| JKA | Tubes, vials, systems, serum separators, blood collection | 5 |
| FPA | Set, administration, intravascular | 5 |
Use these as the dimensions to specify in a tender line.
No closely related category with 50+ devices.
61 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Luer-ended blood collection tube spike", from 14 companies. The largest labeler is Promisemed Medical Devices Inc. with 49% of records.
FMI (Needle, Hypodermic, Single Lumen), JKA (Tubes, Vials, Systems, Serum Separators, Blood Collection), FPA (Set, Administration, Intravascular), 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.