A group of rechargeable batteries held within a holder, container, or mobile cart/trolley intended to provide temporary electrical energy to operate a medical device, typically when it is not possible, intentional, or convenient to connect the device being pow
| Company | Devices | Share |
|---|---|---|
| R & D Batteries, Inc. | 781 | 38% |
| Unipower Corporation | 618 | 30% |
| Anybattery, Inc | 168 | 8% |
| Interstate All Battery Center | 61 | 3% |
| Alpha Source Inc. | 58 | 3% |
| Stryker Corporation | 39 | 2% |
| Fujifilm Sonosite, Inc. | 39 | 2% |
| Med-El Elektromedizinische Geräte Gesellschaft M.B.H. | 30 | 1% |
| Cochlear Limited | 21 | 1% |
| Shenzhen Mindray Bio-Medical Electronics Co., Ltd. | 20 | 1% |
| Resmed Pty Ltd | 16 | 1% |
| Icu Medical, Inc. | 15 | 1% |
Company = labeler of record on GUDID. 72 companies in total; top 12 shown. Click headers to sort.
Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.
| Code | Name | Devices |
|---|---|---|
| LDD | Dc-Defibrillator, Low-Energy, (Including Paddles) | 626 |
| FCO | BOX, BATTERY, RECHARGEABLE | 333 |
| MOQ | Battery, Replacement, Rechargeable | 304 |
| HGM | System, monitoring, perinatal | 137 |
| IYX | Camera, scintillation (gamma) | 104 |
| BTA | PUMP, PORTABLE, ASPIRATION (MANUAL OR POWERED) | 104 |
Use these as the dimensions to specify in a tender line.
2,048 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Portable/mobile rechargeable battery pack", from 72 companies. The largest labeler is R & D Batteries, Inc. with 38% of records.
LDD (Dc-Defibrillator, Low-Energy, (Including Paddles)), FCO (BOX, BATTERY, RECHARGEABLE), MOQ (Battery, Replacement, Rechargeable), HGM (System, monitoring, perinatal)
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.