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Device Explorer · FDA GUDID · GMDN 31072

Personal device holder, single-use

A portable, flexible device designed to hold a portable medical device (e.g., long-term recorder, portable oxygen equipment, urine collection bag, tracheostoma protector) during ambulation or sleep; it is neither designed to hold an invasive tube/catheter to t

US‑registered devices71in commercial distribution
Companies24labelers on GUDID
Single‑use93%of device records
Sterile6%labelled sterile
Prescription63%Rx‑only share
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Share of device records

Westmed, Inc.2028%
Precision Dynamics Corporation68%
Kci Usa, Inc.57%
Medtronic, Inc.57%
O&M Halyard, Inc.57%
Neotech Products Llc46%
Cardinal Health 200, Llc34%
Sunmed, Llc34%

Top labelers

CompanyDevicesShare
Westmed, Inc.2028%
Precision Dynamics Corporation68%
Kci Usa, Inc.57%
Medtronic, Inc.57%
O&M Halyard, Inc.57%
Neotech Products Llc46%
Cardinal Health 200, Llc34%
Sunmed, Llc34%
Fukuda Denshi Co.,Ltd.23%
Somavac Medical Solutions, Inc.23%
Ge Healthcare Finland Oy23%
Resource Optimization & Innovation, L.L.C.23%

Company = labeler of record on GUDID. 24 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

FUKUDA DENSHIAcanthusGuardianSOMAVAC Belt ExtenderSOMAVAC BeltAMCSNAP™SenzaNeoGlo®Suction Caddy (N245)Tubing OrganizerAVELLEN/ANATubeCatchTube Tackles

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

FDA product codes

CodeNameDevices
JAYSupport, Breathing Tube26
MDMINSTRUMENT, MANUAL, SURGICAL, GENERAL USE7
FMPProtector, Skin Pressure6
MDMInstrument, Manual, Surgical, General Use6
OKONegative Pressure Wound Therapy Non-Powered Suction Apparatu5
LGWSTIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF4

GMDN & GCC registration

  • GMDN code 31072 · non‑implantable
  • Single‑use 93% · sterile 6% · Rx‑only 63% · OTC 14%
  • 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 personal device holder, single-use products are registered in the US?

71 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Personal device holder, single-use", from 24 companies. The largest labeler is Westmed, Inc. with 28% of records.

Which FDA product codes apply?

JAY (Support, Breathing Tube), MDM (INSTRUMENT, MANUAL, SURGICAL, GENERAL USE), FMP (Protector, Skin Pressure), MDM (Instrument, Manual, Surgical, General Use)

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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