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Device Explorer · FDA GUDID · GMDN 67106

Multiple physiological parameter monitoring support kit

A collection of noninvasive devices intended to be used in conjunction with a parent physiological parameter monitor for enabling measurement of multiple vital parameters [e.g., electrocardiogram (ECG), noninvasive blood pressure (NIBP), temperature]. It typic

US‑registered devices66in commercial distribution
Companies1labelers on GUDID
Single‑use3%of device records
Sterile0%labelled sterile
Prescription41%Rx‑only share
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Share of device records

Fysicon B.V.66100%

Top labelers

CompanyDevicesShare
Fysicon B.V.66100%

Company = labeler of record on GUDID. 1 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

BOSTON FFR Connection KitABBOTT FFR Connection KitVolcano (Philips) FFR Connection KitACIST FFR Connection KitIR, 5-Lead, AHA, Basic Monitoring KitIR, 5-Lead, IEC, Basic Monitoring KitCardiac, 10-Lead, AHA, Basic Monitoring KitCardiac, 10-Lead, IEC, Basic Monitoring KitQMAPP

Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.

FDA product codes

CodeNameDevices
DSACable, Transducer And Electrode, Patient, (Including Connect66

GMDN & GCC registration

  • GMDN code 67106 · non‑implantable
  • Single‑use 3% · sterile 0% · Rx‑only 41% · OTC 0%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

No structured size data on the register.

Use these as the dimensions to specify in a tender line.

No closely related category with 50+ devices.

How many multiple physiological parameter monitoring support kit products are registered in the US?

66 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Multiple physiological parameter monitoring support kit", from 1 companies. The largest labeler is Fysicon B.V. with 100% of records.

Which FDA product codes apply?

DSA (Cable, Transducer And Electrode, Patient, (Including Connect)

Is this the same as UAE/GCC registration?

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.

How do I get quotes?

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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.

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