VATS BATTERYLithium Polymer Battery Manufacturer
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LiPo batteries for medical devices

Medical devices need batteries that are documented, consistent and traceable. This page explains what to ask for; it makes no medical compliance promise for any product.

Since 2011681 models across 11 families512 Li-polymer modelsCustomers in 30+ countries every year (company profile states)500,000 pcs/day capacity (company profile states)ISO9001 / ISO14001, UL, CE, IEC62133, CB, KC, RoHS — Certificates available upon request
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length (mm) width POUCH CELL diagram, not a photograph

Dimension-callout pouch outline — the site's recurring diagram motif. It is a schematic, not a photograph of a product, factory or customer project.

Home / Applications

Medical applications in the listings include medical equipment packs, miniature medical devices and portable instruments. The representative pack is the 603048-3S, an 11.1 V, 900 mAh lithium polymer pack listed for medical equipment, with its own minimum order, enquiry range and lead time for the listing this page cites. Other medical listings differ in voltage, capacity and terms, and the certificate set for each must be confirmed for that model.

The most important medical-battery question is documentation, not headline capacity. Ask for the certificate set for the exact model, the pack's protection design, the cell traceability the supplier can provide, and the change-notification practice — what happens, and who is told, if a cell or protection component changes. A medical device's own regulatory file depends on its components staying as qualified, so a silent substitution is a serious problem even if the replacement cell looks equivalent.

This page deliberately makes no claim that any product complies with any medical-device regulation or standard. Compliance is a property of the finished device and its regulatory file, not of a battery listing, and a battery supplier's certificate names do not transfer into a device approval. Raise the regulatory questions with the supplier and with your own regulatory advisers before design freeze, and treat certificates as available upon request for the exact model.