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 catalogue configuration for discussion during equipment battery selection. Provide the device safety requirements, load profile and charging arrangement before evaluation.
Source review: 4 November 2026 · No inventory or price is implied.
| Parameter | Published reference |
|---|---|
| Catalogue voltage class | 14.8V |
| Catalogue capacity class | 3.4Ah |
| Chemistry | Lithium-ion |
| 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.
For medical equipment battery projects, the most useful RFQ connects the published reference to the equipment and the project.
Device voltage window, measured duty cycle and low-battery transitions. Include measured peak duration and the target operating time.
Battery identification, protection behavior and monitoring signals. Add the available dimensions, cable direction and the equipment drawing.
State the sample stage, expected quantities, destination market and documents required for review.
Use the collection’s practical guides to prepare a more focused engineering discussion.
Help a device team communicate operating modes, power continuity, cleaning constraints and validation needs to a battery supplier.
Read the technical guideDefine a measurable battery runtime requirement and connect it to device operating modes, replacement planning and controlled validation.
Read the technical guideKeep component specifications, traceability, report scope and device-level responsibilities clear during battery procurement.
Read the technical guideShare the load, dimensions and intended use. Ask for a current model specification and a project review.