A band-like device that has an inflatable bladder in an inelastic sleeve with one or two connecting tubes with connector (typically locking connectors) that can be connected to a mechanism for inflating and deflating the bladder and/or a sphygmomanometer or a
| Company | Devices | Share |
|---|---|---|
| Unimed Medical Supplies, Inc. | 558 | 24% |
| Salter Labs | 420 | 18% |
| Orantech Inc. | 291 | 13% |
| Medline Industries, Inc. | 281 | 12% |
| Statcorp Medical | 269 | 12% |
| Shenzhen Vistar Medical Supplies Co.,Ltd. | 120 | 5% |
| Cables And Sensors, Llc | 75 | 3% |
| Suzhou Minhua Medical Apparatus Supplies Co., Ltd. | 32 | 1% |
| Apk Technology Co.,Ltd. | 28 | 1% |
| Shenzhen Caremed Medical Technology Co., Ltd. | 24 | 1% |
| Reprocessing Products Corporation | 16 | 1% |
| Shenzhen Mindray Bio-Medical Electronics Co., Ltd. | 15 | 1% |
Company = labeler of record on GUDID. 34 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 |
|---|---|---|
| DXQ | blood pressure cuff | 1,280 |
| DXQ | Blood Pressure Cuff | 1,267 |
| MHX | MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR | 17 |
| DXN | System, Measurement, Blood-Pressure, Non-Invasive | 16 |
| DXN | System, measurement, blood-pressure, non-invasive | 14 |
| MWI | Monitor,Physiological,Patient(Without Arrhythmia Detection O | 14 |
Use these as the dimensions to specify in a tender line.
2,305 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Blood pressure cuff, single-use", from 34 companies. The largest labeler is Unimed Medical Supplies, Inc. with 24% of records.
DXQ (blood pressure cuff), DXQ (Blood Pressure Cuff), MHX (MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR), 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.