An electrically-powered device designed to noninvasively measure blood pressure using a self-contained software program that regulates automatic arm/wrist-cuff inflation and measurement cycles. It typically displays current heart rate and mean arterial pressur
| Company | Devices | Share |
|---|---|---|
| Shenzhen Urion Technology Co., Ltd | 426 | 20% |
| Shenzhen Jamr Technology Co., Ltd. | 134 | 6% |
| Alicn Medical Shenzhen, Inc. | 106 | 5% |
| Shenzhen Jiacom Technology Co., Ltd | 84 | 4% |
| Guangdong Transtek Medical Electronics Co.,Ltd | 75 | 4% |
| Joytech Healthcare Co.,Ltd | 64 | 3% |
| Veridian Healthcare Llc | 64 | 3% |
| Shenzhen Pango Electronic Co., Ltd. | 60 | 3% |
| Omron Healthcare, Inc. | 50 | 2% |
| Dongguan E-Test Technology Co.,Ltd | 41 | 2% |
| Beijing Choice Electronic Technology Co., Ltd. | 38 | 2% |
| Welch Allyn, Inc. | 38 | 2% |
Company = labeler of record on GUDID. 178 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 |
|---|---|---|
| DXN | System, Measurement, Blood-Pressure, Non-Invasive | 2,103 |
| DQA | Oximeter | 27 |
| DXN | System, measurement, blood-pressure, non-invasive | 21 |
| DXN | SYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE | 17 |
| NBW | System, Test, Blood Glucose, Over The Counter | 7 |
| QXY | Oscillometric-Based, Over-The-Counter, Atrial Fibrillation N | 6 |
Use these as the dimensions to specify in a tender line.
2,118 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Automatic-inflation electronic sphygmomanometer, portable, arm/wrist", from 178 companies. The largest labeler is Shenzhen Urion Technology Co., Ltd with 20% of records.
DXN (System, Measurement, Blood-Pressure, Non-Invasive), DQA (Oximeter), DXN (System, measurement, blood-pressure, non-invasive), DXN (SYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE)
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.