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Device Explorer · FDA GUDID · GMDN 61393

Multiple active implantable device programmer

An external, portable, non-dedicated, electrically-powered device intended to change, noninvasively (i.e., wirelessly), the operating parameters (programs) of multiple types of implanted electronic devices (e.g., multiple types of pulse generators); it may in

US‑registered devices200in commercial distribution
Companies7labelers on GUDID
Single‑use0%of device records
Sterile0%labelled sterile
Prescription100%Rx‑only share
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Share of device records

Medtronic, Inc.15376%
St. Jude Medical, Inc.2412%
Advanced Neuromodulation Systems, Inc.84%
Stimwave Technologies Incorporated84%
Greatbatch Ltd42%
Thoratec Corporation21%
Medtronic Sofamor Danek, Inc.10%

Top labelers

CompanyDevicesShare
Medtronic, Inc.15376%
St. Jude Medical, Inc.2412%
Advanced Neuromodulation Systems, Inc.84%
Stimwave Technologies Incorporated84%
Greatbatch Ltd42%
Thoratec Corporation21%
Medtronic Sofamor Danek, 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)

Proclaim™Infinity™NeuroSphere™NAHeartMate Touch™Merlin™BurstDR™Prodigy™SJM™Rapid Programmer™Genesis™SJM MRI Activator™Wi-Fi™Eon™Algovita®Wearable Antenna Assembly/StimQ Wearable Antenna

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

FDA product codes

CodeNameDevices
LGWSTIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF67
PJSStimulator, electrical, implanted, for essential tremor59
OLMDeep brain stimulator for obsessive compulsive disorder (OCD51
EZWStimulator, electrical, implantable, for incontinence48
QRBStimulator, spinal-cord, totally implanted for relief of pai47
MRUimplanted subcortical electrical Stimulator (motor disorders46

GMDN & GCC registration

  • GMDN code 61393 · non‑implantable
  • Single‑use 0% · sterile 0% · Rx‑only 100% · 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

Length (Centimeter) · 11Length (Inch) · 11

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

How many multiple active implantable device programmer products are registered in the US?

200 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Multiple active implantable device programmer", from 7 companies. The largest labeler is Medtronic, Inc. with 76% of records.

Which FDA product codes apply?

LGW (STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF), PJS (Stimulator, electrical, implanted, for essential tremor), OLM (Deep brain stimulator for obsessive compulsive disorder (OCD), EZW (Stimulator, electrical, implantable, for incontinence)

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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