Lithium battery imports require UN38.3 test evidence, correct IATA classification (Section II vs Section IA), and configuration-specific packaging. Aplash reviews the manufacturer's accredited-lab UN38.3 certificate, confirms watt-hour and lithium-content thresholds, and acts as named Importer of Record under 関税法 (Customs Act).
Request Assessment| Configuration | Section II (passenger-aircraft acceptable) | Section IA (cargo-only, carrier waiver) |
|---|---|---|
| Watt-hour rating | ≤100 Wh per cell | Above 100 Wh per cell |
| Lithium-metal content | ≤2 g per cell | Above 2 g per cell |
| Aplash IOR position | Standard pricing band | Complex pricing band; carrier confirmation required |
Standard Section II (single SKU, equipment-contained, ≤100 Wh cells): from $2,800 per shipment. Section IA, loose cells, multi-SKU, or air-cargo-only configurations: from $4,800 per shipment.
Customs duties and Japanese consumption tax (JCT) pass through at cost. Aplash earns no margin on the goods, only on the service.
UN38.3 is the United Nations test standard (ST/SG/AC.10/11/Rev.7) covering eight performance tests required for the transport of lithium cells and batteries. Aplash reviews the manufacturer's accredited-lab certificate before customs filing.
Section II covers smaller lithium cells (≤100 Wh, ≤2 g lithium) acceptable on passenger aircraft with standard packaging. Section IA covers larger or higher-energy cells, often forbidden on passenger aircraft or requiring carrier waiver and cargo-only routing.
Damaged, defective, or recalled batteries (UN3090, UN3091 with damage indicators) require specialized waste-classified handling outside Aplash's standard IOR scope. We coordinate referrals to specialized hazardous-waste partners.
UN38.3 does not formally expire, but configuration changes (cell chemistry, packaging, capacity) invalidate the report. Accredited labs typically refresh certificates every 4 to 5 years. Aplash flags expiry risk during the engagement review.
Packed-with-equipment and contained-in-equipment configurations are routinely handled. The underlying device may bring additional regulation (薬機法 (Pharmaceutical and Medical Device Act) for medical, PSE (電気用品安全法) for IT) that Aplash coordinates in parallel.
Aplash sequences customs filing only after the UN38.3 evidence and IATA section classification are confirmed. Engagement starts with a manufacturer-document review at no cost.
Request a no-cost commodity assessment. We confirm IOR feasibility and quote against the public pricing band before any commitment.
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