Define the device context
Describe the intended use, operating environment and the battery's role within the device risk assessment.
Battery catalogue reference for engineering evaluation. This image does not establish approval for a medical device or medical certification.
A higher-capacity three-series candidate for an engineering discussion. The battery and the complete device require their own documented safety and performance assessment.
Source review: 4 November 2026 · No inventory or price is implied.
| Parameter | Published reference |
|---|---|
| Catalogue voltage | 11.1V |
| Catalogue capacity | 10Ah |
| Configuration | 3S2P |
| Listed cell family | Samsung 50E |
| Application approval | Project-specific evaluation |
For medical equipment battery projects, work through these requirements before finalizing the battery choice.
Describe the intended use, operating environment and the battery's role within the device risk assessment.
Confirm electrical limits, protection behavior, thermistor signals, identification and communication as applicable.
Agree test evidence, traceability and change control with the equipment manufacturer. A catalogue reference is not device approval.
Request the current electrical specification, a mechanical drawing, protection limits and test conditions. Where required, ask for the exact model’s transport and safety documentation. Confirm the report holder, model scope and revision.
A company certificate, a cell report and a finished-pack report cover different things. The documents need to match the product and its intended use.
The published values are an initial reference. Compatibility depends on the operating voltage window, continuous and peak current, charging system, enclosure and application requirements. Share those details for a model-specific review.
Send the reference name and your project specification. The team can confirm the available configuration, sample terms, quantity, price and lead time. No standard MOQ or delivery promise is asserted on this page.
Provide device type, intended environment, voltage window, measured current profile, runtime target, enclosure drawing and the required documentation.
Not a claim of medical-device certification or approval. No IEC 60601/ISO 13485 certification has been verified.
Source paths may redirect following the corporate website’s reorganization. Ask Jetray for the current approved model sheet when a legacy page has moved.
Share the load, dimensions and intended use. Ask for a current model specification and a project review.