A mains electricity (AC-powered) device designed to receive continuous, interval and/or spot-check physiological data (e.g., vital signs) from one or more bedside patient monitor(s) (not included) to display this information at a central patient monitoring sta
| Company | Devices | Share |
|---|---|---|
| Welch Allyn, Inc. | 211 | 54% |
| Nihon Kohden Digital Health Solutions, Llc | 31 | 8% |
| Clinicomp International, Inc. | 19 | 5% |
| Philips Medizin Systeme Böblingen Gmbh | 18 | 5% |
| Nihon Kohden Corporation | 15 | 4% |
| Fukuda Denshi Co.,Ltd. | 15 | 4% |
| Nihon Kohden America, Inc. | 15 | 4% |
| Philips Medical Systems Hsg | 14 | 4% |
| Shenzhen Mindray Bio-Medical Electronics Co., Ltd. | 7 | 2% |
| Draeger Medical Systems, Inc. | 7 | 2% |
| Spacelabs Healthcare (Washington), Inc | 7 | 2% |
| Athena Gtx, Inc. | 5 | 1% |
Company = labeler of record on GUDID. 24 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 |
|---|---|---|
| MHX | MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR | 258 |
| MHX | Monitor, Physiological, Patient(With Arrhythmia Detection Or | 183 |
| DSI | Detector And Alarm, Arrhythmia | 49 |
| DPS | Electrocardiograph | 43 |
| MWI | Monitor, physiological, patient (without arrhythmia detectio | 23 |
| HGM | System, Monitoring, Perinatal | 20 |
Use these as the dimensions to specify in a tender line.
389 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Centralized patient monitor", from 24 companies. The largest labeler is Welch Allyn, Inc. with 54% of records.
MHX (MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR), MHX (Monitor, Physiological, Patient(With Arrhythmia Detection Or), DSI (Detector And Alarm, Arrhythmia), DPS (Electrocardiograph)
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.