An electrically-powered device intended to be used to separate the components of multiple types and various volumes of clinical suspensions using centrifugal force. It is a self-contained unit with an electric motor, a vertical shaft, and a horizontal rotor at
| Company | Devices | Share |
|---|---|---|
| Drucker Diagnostics | 492 | 68% |
| Thermo Electron Led Gmbh | 94 | 13% |
| Changsha Yingtai Instrument Co., Ltd | 35 | 5% |
| Lw Scientific, Inc. | 31 | 4% |
| Globe Scientific Inc. | 20 | 3% |
| Andreas Hettich Gmbh | 19 | 3% |
| Biobase Biodustry(Shandong)Co., Ltd. | 9 | 1% |
| Hbh Biotechnology Limited | 4 | 1% |
| Medtox Diagnostics, Inc. | 4 | 1% |
| Fisher Scientific Company L.L.C. | 3 | 0% |
| Arthrex, Inc. | 2 | 0% |
| Bsl Co.,Ltd | 2 | 0% |
Company = labeler of record on GUDID. 21 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 |
|---|---|---|
| JQC | Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use | 741 |
| KSO | Centrifuge, Blood-Bank For In Vitro Diagnostic Use | 32 |
| JQC | CENTRIFUGES (MICRO, ULTRA, REFRIGERATED) FOR CLINICAL USE | 7 |
| PBC | Manual Blood Grouping And Antibody Test Systems | 1 |
| GKG | Centrifuge, Hematocrit | 1 |
| PMQ | Peripheral Blood Processing Device For Wound Management | 1 |
Use these as the dimensions to specify in a tender line.
724 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "General-purpose centrifuge IVD", from 21 companies. The largest labeler is Drucker Diagnostics with 68% of records.
JQC (Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use), KSO (Centrifuge, Blood-Bank For In Vitro Diagnostic Use), JQC (CENTRIFUGES (MICRO, ULTRA, REFRIGERATED) FOR CLINICAL USE), PBC (Manual Blood Grouping And Antibody Test Systems)
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.