Hi9Bot’s far-infrared platform is backed by third-party laboratory testing. Reports are shared with buyers during sourcing and can be referenced in your market’s compliance documentation workflow.
Far-Infrared Emissivity — 0.89
| Parameter | Far-infrared emissivity 0.89 (standard requires > 0.88) — Pass |
|---|---|
| Method | GB/T 30127-2013, Clause 7.1 |
| Issued by | National Quality Inspection and Testing Center for Infrared and Industrial Electrothermal Products (Wuhan Inspection, Testing and Certification Development Group) |
| Report No. | (2026) WT-HWCD-0494 |
Emissivity & Wavelength Band — 7–13 μm
| Parameter | Normal total emissivity 0.89 at 45°C (requires > 0.83); effective radiation concentrated in the 7–13 μm band (> 50% of total radiant energy) — Compliant |
|---|---|
| Method | GB/T 7286-2008, Clause 9 |
| Issued by | National Quality Inspection and Testing Center for Infrared and Industrial Electrothermal Products |
| Report No. | (2026) WT-HWCD-01059 |
Antiviral Laboratory Result (In-Vitro)
| Parameter | Virus inactivation rate > 99.99% against Influenza A (H1N1) in laboratory testing — in-vitro result |
|---|---|
| Method | Reference ISO 18184:2019 |
| Issued by | Gmicro Testing / Guangdong Detection Center of Microbiology |
| Report No. | 2021FM03948R001 |
US & EU Market Compliance Path
Heat therapy devices entering the US and EU carry destination-market requirements beyond factory test reports. Our compliance matrix is shared openly with buyers:
| Requirement | Status | Note |
|---|---|---|
| FIR emissivity & wavelength (GB/T 30127 / GB/T 7286) | In hand — reports shared | 0.89 emissivity; 7–13 μm band; report numbers above |
| Antiviral lab result (ISO 18184 reference) | In hand — report shared | In-vitro result; material-level documentation |
| CE / UKCA pathway (EMC, LVD, RoHS) | Arranged per order | We coordinate testing through partner labs; cost and lead time quoted with your order |
| FCC Part 15 (US, electronic models) | Arranged per order | Applies to USB/battery heated SKUs with electronics |
| UN38.3 + lithium air-freight docs (battery SKUs) | Arranged per order | Battery specification and test docs supplied with shipment file |
| UL / ETL (IEC 60335 style evaluation) | By project scope | Mainly for 170–210 W mains-powered foot warmers; scope with us before ordering |
| Prop 65 (California) | By project scope | Material declarations available; labeling per your channel |
Compliance Notes for Importers
- Hi9Bot products are consumer wellness products designed for warmth, relaxation and comfort. They are not medical devices and are not intended to diagnose, treat, cure or prevent any disease.
- Medical device qualification registration is in progress for selected professional-line products; contact us for current status before making market-specific claims.
- We support buyers with documentation workflows for destination-market requirements (CE/UKCA/RoHS pathways, lithium-battery air freight documents for battery SKUs).
- Sample policy: samples ship with courier collect; sample fees are credited against your first bulk order.
Need the reports for your compliance file?
Request the test report package (PDF) through the inquiry form.
Request the test report package (PDF) through the inquiry form.