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Device Explorer · FDA GUDID · GMDN 30087

Vulnerable patient home alert system

An assembly of electronic devices designed to provide an alarm signal to summon help when activated in response to a patient’s need for urgent assistance or care (e.g., epileptic seizures, falls, low insulin levels). It typically consists of user- or sensor-ac

US‑registered devices230in commercial distribution
Companies7labelers on GUDID
Single‑use15%of device records
Sterile0%labelled sterile
Prescription0%Rx‑only share
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Share of device records

Alimed, Inc.10445%
Lifeline Systems Company7733%
Securitas Healthcare Llc4319%
Rescue Alert21%
Drive Devilbiss Healthcare21%
Vive Health Llc10%
Medline Industries, Inc.10%

Top labelers

CompanyDevicesShare
Alimed, Inc.10445%
Lifeline Systems Company7733%
Securitas Healthcare Llc4319%
Rescue Alert21%
Drive Devilbiss Healthcare21%
Vive Health Llc10%
Medline Industries, Inc.10%

Company = labeler of record on GUDID. 7 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

HomeSafe Standard Personal Help WriststrapHomeSafe Standard Personal Help PendantSenior Living Personal Help Device WriststrapSenior Living Personal Help Device PendantSenior Living Alert Device Personal Help WriststGoSafe / HomeSafe Personal Help WriststrapSenior Living Alert Device Personal Help PendantGoSafe / HomeSafe Personal Help PendantSenior Living Alert Device AutoAlertHomeSafe AutoAlert PendantSenior Living Alert Device AutoAlert with IndicaGoSafe / HomeSafe AutoAlert PendantPhilips BlueBandHomeSafe (Wireless) Home CommunicatorHomeSafe Standard Home CommunicatorPhilips GoSafe 2

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

FDA product codes

CodeNameDevices
KMIMONITOR, BED PATIENT146
ILQSystem, communication, powered91
KMIMonitor, Bed Patient15
IQBBELT, WHEELCHAIR1
IMXBOARD, LAP, WHEELCHAIR1

GMDN & GCC registration

  • GMDN code 30087 · non‑implantable
  • Single‑use 15% · sterile 0% · Rx‑only 0% · OTC 80%
  • 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.

How many vulnerable patient home alert system products are registered in the US?

230 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Vulnerable patient home alert system", from 7 companies. The largest labeler is Alimed, Inc. with 45% of records.

Which FDA product codes apply?

KMI (MONITOR, BED PATIENT), ILQ (System, communication, powered), KMI (Monitor, Bed Patient), IQB (BELT, WHEELCHAIR)

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.

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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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