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Device Explorer · FDA GUDID · GMDN 34158

Secondary battery

A rechargeable set of electrochemical cells, or a single cell, designed to store chemical energy and release it in the form of electrical energy to provide power for active implantable medical devices or external medical instruments, for backup power for progr

US‑registered devices356in commercial distribution
Companies25labelers on GUDID
Single‑use1%of device records
Sterile0%labelled sterile
Prescription36%Rx‑only share
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Share of device records

Advanced Bionics, Llc13438%
Artisan Power Llc7521%
Cochlear Limited4011%
Zoll Circulation, Inc.3510%
Thoratec Corporation206%
Alpha Source Inc.93%
Breas Medical Ab51%
Vapotherm, Inc.51%

Top labelers

CompanyDevicesShare
Advanced Bionics, Llc13438%
Artisan Power Llc7521%
Cochlear Limited4011%
Zoll Circulation, Inc.3510%
Thoratec Corporation206%
Alpha Source Inc.93%
Breas Medical Ab51%
Vapotherm, Inc.51%
Riverpoint Medical, Llc41%
Medtronic, Inc.41%
Advanced Bionics Ag41%
Smith & Nephew, Inc.31%

Company = labeler of record on GUDID. 25 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Vivo 45 LSVivo 50, VIvo 65HeartMate™NAswiftPro Battery PackNihon Kohden SVM-7200 Series Vital Signs Monitorn.a.DYONICSQBC DiagnosticsAutoPulse Li-ion Battery™AutoPulse BatteryVapothermKlaxonMedLED ChromeMedLED Onyx SapphireMedLED Spectra

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

FDA product codes

CodeNameDevices
MCMImplant, cochlear151
MCMIMPLANT, COCHLEAR115
MOQBattery, Replacement, Rechargeable92
MCMImplant, Cochlear50
DRMCompressor, Cardiac, External35
DSQVentricular (Assisst) Bypass18

GMDN & GCC registration

  • GMDN code 34158 · non‑implantable
  • Single‑use 1% · sterile 0% · Rx‑only 36% · 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.

How many secondary battery products are registered in the US?

356 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Secondary battery", from 25 companies. The largest labeler is Advanced Bionics, Llc with 38% of records.

Which FDA product codes apply?

MCM (Implant, cochlear), MCM (IMPLANT, COCHLEAR), MOQ (Battery, Replacement, Rechargeable), MCM (Implant, Cochlear)

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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