A tube intended to be used in the laboratory to contain a clinical specimen, reagent, or other material associated with in vitro diagnostic testing, for separation by centrifugation. It is designed to be placed in a centrifuge rotor for the procedure; it may a
| Company | Devices | Share |
|---|---|---|
| Sartorius Stedim Lab Limited | 23 | 24% |
| Kova International, Inc. | 17 | 18% |
| Globe Scientific Inc. | 12 | 12% |
| Dynarex Corporation | 10 | 10% |
| Yancheng Jingwei Chemicals Co., Ltd | 9 | 9% |
| Alltrista Plastics Llc | 9 | 9% |
| Cardinal Health 200, Llc | 6 | 6% |
| Kb Medical (Group), Inc. | 3 | 3% |
| Stemcell Technologies Canada Inc | 2 | 2% |
| Typenex Medical Llc | 2 | 2% |
| Sakura Finetek U.S.A., Inc. | 1 | 1% |
| Drg Instruments Gesellschaft Mit Beschränkter Haftung | 1 | 1% |
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 |
|---|---|---|
| JJH | Clinical Sample Concentrator | 26 |
| NNK | Container, Specimen Mailer And Storage, Non-Sterile | 20 |
| JQC | Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use | 10 |
| LGX | Table, Examination, Medical, Powered | 9 |
| FMH | Container, Specimen, Sterile | 7 |
| FMH | CONTAINER, SPECIMEN, STERILE | 6 |
Use these as the dimensions to specify in a tender line.
97 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Centrifuge tube IVD", from 14 companies. The largest labeler is Sartorius Stedim Lab Limited with 24% of records.
JJH (Clinical Sample Concentrator), NNK (Container, Specimen Mailer And Storage, Non-Sterile), JQC (Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use), LGX (Table, Examination, Medical, Powered)
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.