A custom lithium-ion battery for your medical equipment

Batteries Prod designs and manufactures custom batteries in Monteux, from specification to series production. Role, runtime, integration, BMS and validation shape each architecture.

Infusion pumps and medical monitors
The battery role and operating scenario guide the pack architecture.
Since 2013
Lithium battery development and manufacturing
100 MWh
Annual production capacity
ISO 9001
Company certified since 2021
250,000
Batteries manufactured

What we define together

Six sets of information are enough to outline an initial architecture. Partial data already helps identify what needs to be completed.

Send my initial project data

Use

Battery role

Main power, backup source or another scenario to be defined.

Runtime

Cycles and charging

Target duration, idle periods, charging frequency and available charging periods.

Electrical

Voltage, current and power

Consumption, continuous and peak current, power and charging characteristics.

Integration

Weight, volume and connectors

Available space, mounting, target weight, cable exits, connectors and operating conditions.

System

Interfaces and BMS

Protection, signals, communication, status and interaction with the equipment and charger.

Project

Requirements and volumes

Target market, tests, documents, prototypes, annual volumes and schedule.

Three families of medical equipment

Use and integration vary by equipment. The battery is defined for the actual system, never for a generic category.

  • Medical beds

    Movement or adjustment cycles, charging, integration and battery role.

  • Electronic medical equipment

    Power, interfaces and status information considered across the complete system.

  • Mobile medical equipment

    Available space, connectors, charging, movement and operating environment.

Main power or backup source: what changes

Architecture choices depend on when the battery operates and which functions it powers.

One specification, two scenarios

Use, electrical data, integration, interfaces, requirements and volumes.

Main power

The battery powers the equipment during normal operation. Sizing depends on the operating profile and charging cycle.

  • Operating profile and target period between charges
  • Continuous current, power peaks and charging method
  • Interfaces with the equipment, BMS and status indication

Backup source

The battery operates under a backup scenario defined with the manufacturer. The scenario sets when it starts and which functions it powers.

  • Conditions that trigger backup operation and functions to power
  • Target duration, charging strategy and expected availability
  • Status indication, diagnostics and expected system behaviour

Runtime, behaviour and acceptance criteria are defined and verified for the intended scenario.

An architecture defined for the complete system

Cells, mechanics, connectors, electronics and the BMS are considered with the equipment. Each choice affects the others.

Cells

Selected for the electrical profile, environment and project objectives.

Mechanics

Enclosure, mounting and access defined for the space available in the equipment.

Connectors

Power, charging, signals and cable exits matched to the intended interfaces.

Electronics

Measurement, protection and control functions developed for the project.

BMS

Battery management, status information and communication defined for the equipment.

See our engineering process
Components being soldered on a battery circuit board
Battery circuit board development by the Batteries Prod engineering team.

Tests, documents and standards defined case by case

The programme depends on the equipment, its use, the target market and the final product's validation route.

See our testing and certification support
Environmental test chambers in a laboratory
The test programme depends on the equipment, its use and target market.
  • Tests

    Conditions and acceptance criteria defined from the project's use and risks.

  • Documents

    Design data, traceability, inspections, reports and requested supporting evidence.

  • Standards

    Applicable texts identified for the final product, its destination and market.

No validation route applies by default. Internal testing does not by itself constitute certification.

From prototype to series production, step by step

Each step checks the battery against the specification before repeatable production is prepared in Monteux.

  1. Prototype

    Check integration and operation with the equipment.

  2. Testing

    Apply the defined programme and document the results.

  3. Industrialisation

    Prepare the production file, assembly operations and inspection equipment.

  4. Series production

    Start manufacturing after the architecture and process are approved.

Operator handling a cell assembly on a production line
Batteries Prod production line in Monteux, France.

Manufactured, traced and tested in Monteux

Series production uses documented operations and controls defined during industrialisation.

  • Manufacturing in France at the Batteries Prod factory
  • Traceability of every battery and its operations
  • Quality controls throughout manufacturing
  • Systematic testing before shipment
Explore our engineering capabilities

Questions before starting a medical battery study

Include the battery role, use, runtime, electrical data, integration, interfaces, market, volumes and schedule. Partial data is enough.

Tell us about your medical equipment

Even with incomplete data, we can qualify the need and agree the next step: feasibility review, study or prototype.

Share my medical project+33 9 82 99 09 59

Speak directly with the Batteries Prod team

Custom Lithium Batteries for Medical Equipment - Batteries Prod