A small unit dedicated to making communication possible between the patient monitoring system and other independent devices (e.g., ventilator, infusion pump, gas analyser, display monitors) connected to the same patient, creating an interface. It is designed t
| Company | Devices | Share |
|---|---|---|
| Philips North America Llc | 139 | 79% |
| Spacelabs Healthcare (Washington), Inc | 14 | 8% |
| Philips Medizin Systeme Böblingen Gmbh | 7 | 4% |
| Draeger Medical Systems, Inc. | 4 | 2% |
| Terumo Cardiovascular Systems Corporation | 4 | 2% |
| Resmed Pty Ltd | 4 | 2% |
| Elmed Incorporated | 1 | 1% |
| Ge Healthcare Finland Oy | 1 | 1% |
| Icu Medical, Inc. | 1 | 1% |
Company = labeler of record on GUDID. 9 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 |
|---|---|---|
| MWI | Monitor,Physiological,Patient(Without Arrhythmia Detection O | 174 |
| DQA | Oximeter | 97 |
| DXN | System, Measurement, Blood-Pressure, Non-Invasive | 73 |
| MWI | Monitor, Physiological, Patient (Without Arrhythmia Detectio | 72 |
| FLL | Thermometer, Electronic, Clinical | 72 |
| CCK | Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase | 72 |
Use these as the dimensions to specify in a tender line.
175 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Patient monitoring system module, interfacing", from 9 companies. The largest labeler is Philips North America Llc with 79% of records.
MWI (Monitor,Physiological,Patient(Without Arrhythmia Detection O), DQA (Oximeter), DXN (System, Measurement, Blood-Pressure, Non-Invasive), MWI (Monitor, Physiological, Patient (Without Arrhythmia Detectio)
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.