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Device Explorer · FDA GUDID · GMDN 36545

Basic power supply, reusable

A device designed to receive alternating-current energy (AC-power) from a mains electricity power line and deliver one or more regulated direct-current outputs to supply devices with electrical energy. It typically consists of a step-up or step-down transforme

US‑registered devices164in commercial distribution
Companies51labelers on GUDID
Single‑use1%of device records
Sterile0%labelled sterile
Prescription63%Rx‑only share
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Share of device records

Eitan Medical Ltd117%
Zimmer Orthopaedic Surgical Products, Inc.106%
Dabir Surfaces, Inc.106%
Icu Medical, Inc.95%
Physio-Control, Inc.85%
Fujifilm Sonosite, Inc.85%
Athena Gtx, Inc.85%
Mckesson Medical-Surgical Inc.74%

Top labelers

CompanyDevicesShare
Eitan Medical Ltd117%
Zimmer Orthopaedic Surgical Products, Inc.106%
Dabir Surfaces, Inc.106%
Icu Medical, Inc.95%
Physio-Control, Inc.85%
Fujifilm Sonosite, Inc.85%
Athena Gtx, Inc.85%
Mckesson Medical-Surgical Inc.74%
Integra Lifesciences Corporation74%
Thoratec Corporation64%
Welch Allyn, Inc.64%
Omron Healthcare, Inc.64%

Company = labeler of record on GUDID. 51 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

LIFEPAK 15 AC Power AdapterSurgiCountVivo 45 LSWarrior AC StationAC Power supply ModuleCLEANMeniett™ Power SupplyHeartMate™ProVuDe Soutter MedicalRENASYS TOUCH Class I Power SupplyRENASYS TOUCH DEVICE & POWER SUPG-22i-Cut Power Supply Type Ai-Cut Power SupplyWide range power adapter MPR1/2

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

FDA product codes

CodeNameDevices
FNMMattress, Air Flotation, Alternating Pressure14
MRZAccessories, Pump, Infusion12
DQAOximeter11
DXNSystem, Measurement, Blood-Pressure, Non-Invasive10
FQHLAVAGE, JET9
MPDAuxiliary power supply (AC or DC) for low-energy dc-defibril8

GMDN & GCC registration

  • GMDN code 36545 · non‑implantable
  • Single‑use 1% · sterile 0% · Rx‑only 63% · OTC 8%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Length (Feet) · 10

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

How many basic power supply, reusable products are registered in the US?

164 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Basic power supply, reusable", from 51 companies. The largest labeler is Eitan Medical Ltd with 7% of records.

Which FDA product codes apply?

FNM (Mattress, Air Flotation, Alternating Pressure), MRZ (Accessories, Pump, Infusion), DQA (Oximeter), DXN (System, Measurement, Blood-Pressure, Non-Invasive)

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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