电动、带电池或科技类美容设备可能涉及多条监管路径：电子电器、锂电池货物、蓝牙/Wi‑Fi/RF设备、LED/IPL/激光设备、按摩器械，或在具有治疗宣称时可能被认定为医疗器械。判断错误可能导致HS编码错误、缺少电池文件、无法享受C/O优惠、DG订舱受阻或临时触发ICT/医疗器械要求。本文提供一套ETA前审核HS编码、税费、C/O、标签、电池、技术功能及专业监管政策的E2E路径。

适用范围

本文适用于带电、带电池或科技类美容设备，包括洁面仪、按摩仪、LED面罩、IPL/RF/EMS美容仪、蒸脸仪、美发造型电器、带App连接的美容设备以及内置锂电池设备。

主要范围

洁面仪、按摩仪、LED面罩、IPL/RF/EMS设备、蒸脸仪、美发电器、带电池或App连接的美容设备。

不得自动适用

带医疗宣称、旧/翻新设备、样品、保修件、设备+化妆品组合均需单独审核。

控制原则

应按目录、数据表、型号、功能及实际进口目的进行审核。

电动/电池/科技类美容设备进口手续指南示意图 — 产品组及清关前资料审核场景示意。

术语解释与手续重要性

该类产品可能同时涉及化妆品、电子电器、ICT、锂电池运输及医疗器械规则。

术语	业务理解	对手续的影响
电动/电池/科技类美容设备	使用电源、充电电池、传感器、光、热、震动、RF、EMS、App控制或电子配件的美容/个人护理工具。	首先要把设备与成品化妆品区分开；化妆品备案不能替代设备合规。
SDS/MSDS	电池、凝胶、导电液、清洁液或运输风险材料的安全数据表。	用于判断是否需要危险品运输处理。
UN38.3	锂电池运输安全测试。	设备内置或随附锂电池时通常会被要求。
UN3481 / UN3091	锂离子/锂金属电池装在设备内或与设备同包装的运输条目。	影响空运/海运订舱、包装标识和运输文件。
RF / Wi‑Fi / Bluetooth	无线电传输或短距离无线连接功能。	如果HS和货物描述属于清单，可能触发ICT第二类产品合规。
IPL / Laser / LED / RF / EMS	美容护理中的光、脉冲光、激光、射频或电刺激技术。	必须审核宣称：美容护理不同于医疗治疗。
医疗器械	用于诊断、治疗、康复或医疗/生理干预目的的设备。	如有治疗或皮肤医学宣称，可能触发医疗器械监管。
越文附加标签	原标签缺少越南语必备信息时补充的标签。	应包括名称、型号、产地、电气/电池参数、警示及进口责任方。
ETA	预计到港/到机场时间。	用于倒推HS、C/O、电池文件、标签及专业文件的锁定时间。

产品分类与识别

不得仅按“美容仪”商业名称归类。应审核主要功能、电源/电池、作用技术、无线功能、宣称、配件及进口目的。

产品详细分类表

产品组/货物情形	需检查技术特征	型号/功能示例	证明文件	可能触发政策	需对照文件	适用说明
带电池洁面/按摩设备	马达、震动、旋转、电池、USB线/适配器、型号/序列号、接触材质。	洁面仪、硅胶按摩仪、眼部按摩仪。	目录、数据表、标签照片、电池参数、UN38.3。	第85/90章HS、标签、锂电池运输、可能空运DG。	发票、箱单、提单/空运单、目录、电池资料、原标签。	不是化妆品；随附凝胶/精华需另行审核。
LED面罩/光美容设备	波长、功率、红光/蓝光/NIR、控制模式、适配器/电池、宣称。	LED面罩、LED美容棒、光疗美容仪。	目录、数据表、说明书、测试报告。	可能归入8543或有医疗宣称时归入9018；需审核标签及电池。	技术数据、波长、宣称、说明书、标签。	需区分美容护理与医疗治疗。
IPL/激光/RF/EMS设备	能量输出、波长、RF/EMS模式、头部、使用部位、宣称。	家用IPL脱毛仪、RF提拉仪、微电流/EMS美容仪。	能量参数、CE/FCC/IEC、说明书、警示标签。	HS 8543/9018；有治疗宣称可能触发医疗器械。	目录、测试报告、宣称、说明书、标签。	未审核宣称前不得断定无需许可。
蒸脸/加热设备	加热元件、水箱、蒸汽输出、电气参数。	蒸脸仪、纳米喷雾仪。	目录、功率、电压、加热结构、安全警示。	可能为电器类，HS 8516/8543，需审核标签与安全。	目录、原标签、电气参数、测试报告。	不得套用于医疗雾化/吸入设备。
吹风机及热造型工具	电热丝、马达、温度模式、功率、电压。	吹风机、卷发棒、直发器、电热梳。	数据表、电压/功率、安全标准、原标签。	HS 8516；可能需电气安全与标签审核。	目录、测试报告、电气参数、C/O。	如触发能效/质量检验政策需另行审核。
带Wi‑Fi/Bluetooth/App设备	无线模块、频段、发射功率、App功能及数据传输。	智能LED面罩、App美容仪、蓝牙皮肤分析仪。	RF模块数据表、频率、RF测试报告、说明书。	如属清单，可能触发ICT合格认证/声明。	RF数据表、测试报告、模块/标签信息。	仅USB线连接不等于无线触发。
设备+凝胶/精华组合	设备与外用化妆品一起销售。	IPL仪+冷却凝胶，RF仪+导电精华。	INCI、标签、授权/CFS、化妆品备案文件。	可能同时适用设备合规和化妆品备案。	设备资料、化妆品资料、标签、套装规格。	化妆品备案不能替代设备政策审核。
样品/保修/翻新设备	非商业用途、已使用/维修、展示品或保修替换件。	样品美容仪、保修件、翻新设备。	进口目的、保修合同、序列号清单、状态照片。	可能触发旧货、暂进复出、维修或专业审核。	合同、序列号、用途说明、照片。	需区分非销售样品与上市销售货物。

按功能判断政策触发点表

功能/情形	需向供应商索取资料	需核查的手续路径	ETA前控制点
无电池、无无线、无医疗宣称	目录、型号、功率、接触皮肤材质、原标签。	HS、商品标签、C/O，以及如列入目录的电气安全路径。	在最终发票前锁定品名和HS。
内置锂电池	电池规格、Wh额定值、UN38.3、MSDS/SDS、包装方式。	DG运输、空运/海运订舱、包装标识和电池声明。	ETD前锁定运输方案，避免承运人拒收。
Wi‑Fi/蓝牙/RF/APP控制	RF模块、频率、发射功率、测试报告、说明书。	如HS及描述落入现行目录，可能触发ICT第二类/合格评定。	ETA前对照第29/2025/TT-BKHCN号通知及HS/描述。
LED/IPL/激光/RF/EMS	波长、能量、功率、说明书、警示和营销宣称。	HS 8543/9019/9018；如有治疗宣称存在医疗器械风险。	订舱前区分美容宣称与治疗/医疗宣称。
设备附带凝胶/精华/化妆品	INCI、CFS/LOA（如需）、标签、配方、功效。	外用产品需核查化妆品公布；设备路径仍需单独审核。	不能用化妆品公布替代设备合规审核。
样品/保修/翻新货	进口目的、数量、序列号、状态、保修合同。	海关贸易方式、旧/翻新货、标签和许可证（如有）。	报关前说明目的及货物状态。

提示：笼统品名可能导致HS错误、ICT/医疗器械路径错误、漏锂电池文件或设备+化妆品组合处理错误。

HS编码、税费与原产地证

HS归类必须依据实际功能和结构。马达、加热、LED/RF模块、蓝牙App或医疗宣称都可能改变HS及监管路径。

HS编码、税费与C/O建议表

参考HS	适用货物组	归类依据	适用条件	普通进口税	MFN税率	VAT	需核查C/O/FTA	需对照文件
8510	带内置马达的剃须、理发、脱毛工具。	主要功能为通过马达切割/剃除毛发。	适用于马达驱动且非热造型、IPL/激光或医疗设备。	如无单独普通税率，通常按MFN的150%思路核查；需确认8位HS。	按最终HS核查当前MFN。	常见为10%，以报关时VAT政策为准。	核查ATIGA、ACFTA/RCEP、AKFTA/VKFTA/RCEP、VJEPA/AJCEP/CPTPP/RCEP、EVFTA、UKVFTA等。	目录、数据表、标签照片、马达参数、C/O、发票/箱单。
8516.31 / 8516.32	吹风机、卷发/直发器等电热美发工具。	功能依赖电加热或热风。	适用于热造型工具；需与按摩、LED/IPL/RF分开。	通常按MFN的150%核查普通税；查现行税则。	按8位HS、原产地和C/O核查。	常见10%。	C/O描述应匹配吹风机/美发电器。	目录、功率/电压、安全文件、原标签、C/O。
8509.80	如无更具体税目，适用于带内置马达的家用机电器具。	马达驱动的家用/个人护理功能。	仅在8510/8516/9019等更具体税目不适用时使用。	核查现行税则；如医疗或RF功能为主则不适用。	核查最终HS。	常见10%。	按实际原产地核查FTA。	目录、马达结构、功能、照片、C/O。
9019.10	按摩器械，主要功能为按摩。	震动、压缩、机械按摩功能。	如有医疗宣称需转医疗器械审核。	核查现行税则，不按商业名称直接归类。	核查8位HS。	常见10%。	按路线核查C/O/FTA。	目录、说明书、宣称、电池参数、C/O。
8543.70	具有独立功能的电气设备，常见于LED/RF/EMS等特殊美容设备。	未被其他税目具体列明的独立电子功能。	需审核无线模块、电池、医疗宣称、软件/App。	核查现行税则；无线功能可能触发ICT。	核查最终HS。	常见10%。	核查相关FTA；C/O上的HS需可解释。	数据表、框图、RF参数、宣称文件、C/O。
9018.90	如具有医疗或治疗用途的其他医疗仪器。	诊断、治疗、康复或临床/皮肤科用途。	仅在完成医疗器械分类及监管审核后使用。	核查税率及医疗器械进口条件；不适用于普通美容仪。	按最终HS及器械类别核查。	常见10%或按医疗器械税收政策。	核查FTA及C/O一致性。	分类、用途、说明书、技术/临床文件、C/O。
8504.40	适配器、充电器、电源转换器，如单独申报。	AC/DC转换或充电功能。	随设备进口时需判断按套装还是分行申报。	核查现行税则。	核查最终HS。	常见10%。	如单独申报需核查适配器C/O。	适配器数据表、功率标签、套装文件、C/O。
8507 / UN3481运输	单独进口或装在设备中的锂电池。	电池化学体系、Wh、是否装在设备中。	HS适用于电池单独进口；运输规则适用于存在锂电池的货物。	核查税则与电池运输要求。	核查最终HS。	常见10%。	电池单独申报时核查C/O；运输需电池声明。	电池参数、UN38.3、MSDS、包装指令、C/O。
9018.90	如具有医疗、诊断、治疗或皮肤科用途且符合医疗器械特征的设备。	依据预期用途、宣称、说明书、警示、使用环境及医疗器械分类判断。	不适用于纯美容设备；仅在有治疗、诊断、康复或医疗用途时审核。	需核查税则并同步审核医疗器械管理路径。	核查医疗器械分类及最终HS。	通常为10%；如有医疗器械VAT特殊政策需另行核查。	C/O/FTA取决于最终HS；医疗器械资料不能替代C/O。	医疗器械分类、目录、说明书、预期用途、流通文件（如有）、C/O。
9027.89 / 9027.90	皮肤分析仪或以传感器测量水分、油分、色素等指标且测量为主要功能的设备。	主要功能为测量/检测/分析，而非普通美容配件。	技术资料显示测量/分析为主要功能时适用。	按8位HS核查现行税则。	核查最终HS及C/O描述。	通常为10%。	按原产地核查FTA；C/O应与analyzer/measuring instrument描述匹配。	传感器数据表、测量指标、软件界面、照片、C/O。
8504.40 / 8504.90	单独进口或单独列项的适配器、充电器、电源转换器。	主要功能为电源转换/充电；需区分随套装销售的附件与单独进口货物。	如作为零售套装进口，可审核套装处理；如单独进口需单独核HS。	需核查税则；若单独列项，不应并入主设备HS。	按8位HS核查。	通常为10%。	按原产地核查C/O，并要求描述匹配adapter/charger。	发票/装箱单、适配器目录、输入/输出参数、安全文件（如有）。
3304 / 3307	与设备同套销售的导电凝胶、精华或外用护肤品，如本质为化妆品。	属于化妆品/个人护理制剂，而非设备本身。	套装中含外用产品时适用；上市流通可能需要化妆品公布资料。	税费需按相应化妆品HS核查，不能使用设备HS。	按8位化妆品HS核查税则。	通常为10%，以现行VAT政策为准。	按原产地核查FTA；C/O描述需与化妆品一致。	INCI、CFS/LOA（如需）、标签、化妆品公布资料、C/O。

按进口路线核查C/O/FTA表

来源/产地	FTA	C/O格式或原产地文件	如有依据的特别优惠税率	适用条件	需对照文件	适用说明
ASEAN	ATIGA	Form D or valid origin document	May apply if PSR for final HS is satisfied.	Goods description, HS, origin and direct transport must match.	C/O, Invoice, Packing List, B/L, catalogue, model list.	Do not use a device C/O to cover separately declared batteries/adapters unless the description covers them.
China	ACFTA or RCEP	Form E / RCEP C/O or valid origin document	Check preferential tariff by final HS.	Review CTH/CTSH/RVC and third-party invoice if any.	C/O, commercial documents, catalogue, HS on C/O.	Form E is often queried when descriptions are generic or HS differs.
Korea	AKFTA / VKFTA / RCEP	Form AK / VK / RCEP	May apply under the selected agreement.	Choose the agreement with valid proof and best treatment.	C/O, Invoice, B/L, catalogue, origin criteria.	Do not choose FTA only by export country if actual origin differs.
Japan	VJEPA / AJCEP / CPTPP / RCEP	Form VJ / AJ / CPTPP / RCEP	Review tariff schedule by final HS.	PSR, direct transport and origin documents must be satisfied.	C/O, invoice, packing list, transport document.	Technology products with many components require careful PSR review.
EU / UK	EVFTA / UKVFTA	EUR.1 or origin statement if eligible	May apply if origin proof is valid.	Review REX/origin statement, description and transport.	Invoice statement, C/O if any, B/L/AWB, catalogue.	Check shipment value and exporter status for self-certification.
Australia – New Zealand	AANZFTA / CPTPP / RCEP	Form AANZ / CPTPP / RCEP	Review preferential schedule by import lane.	PSR and direct transport must be met.	C/O, B/L, invoice, model list.	Do not group models if the C/O describes only part of the shipment.
India / Hong Kong	AIFTA / AHKFTA	Form AI / AHK or valid origin document	Review each preferential schedule by final HS.	Origin criteria, description and transport must match.	C/O, invoice, B/L/AWB, catalogue.	Transit through third countries requires supporting transport records.

C/O审核清单

检查点	审核要求	错误风险
C/O form	Correct form under the chosen agreement.	Wrong form may lead to denial of preference.
Origin criteria	WO/RVC/CTH/CTSH or other criteria must match PSR for final HS.	Technology devices with many components require stricter PSR review.
Description & HS	Goods description, model, HS, quantity and weight must align with customs declaration and documents.	HS on C/O may differ but must be explainable.
Third-party invoice	If used, the C/O must reflect the agreement’s requirements.	Missing third-party invoice details may trigger verification.
Direct transport	B/L/AWB and transit records must support origin integrity.	Multi-leg transit needs additional proof.
Issuance date & validity	C/O must be issued and submitted within the permitted period.	Expired or late-submitted C/O can lose preference.

资料清单与提交方式

资料应分为商业文件、技术/专业文件，以及如适用的锂电池/DG运输文件。

业务资料清单

文件组	所需文件	用于步骤	准备方	常见错误	ETA前检查
Commercial documents	Commercial Invoice, Packing List, Sales Contract/PO, B/L/AWB, Arrival Notice, C/O if claiming preference.	Customs declaration, valuation, C/O and cargo release.	Importer, Procurement, Docs and Forwarder.	Generic item name, mismatched model/quantity/serial or unclear Incoterms.	Match each line against catalogue, original label and C/O before ETA.
Technical device file	Catalogue, datasheet, user manual, label photos, model/serial list, electrical/battery specs and product structure.	HS classification and policy trigger review.	Supplier, Importer and Compliance team.	Missing battery capacity, RF data, power rating or claims.	Request official PDF files and real label/product photos.
Lithium-battery file	MSDS/SDS, UN38.3, battery spec, Wh rating, packing declaration, PI 966/967 if air.	Air/sea booking, packaging, package marking and DG declaration.	Supplier, Forwarder and DG team.	Battery not declared; spare battery treated as installed battery; missing UN38.3.	Confirm battery configuration before booking.
ICT file if wireless	RF specification, frequency band, output power, test report, module datasheet and applicable QCVN if listed.	Conformity certification/declaration if triggered.	Supplier, Compliance and certification body.	Confusing USB connection with wireless function; missing RF data.	Request RF module datasheet and compare with current ICT Group 2 list.
Medical-device file if claims exist	Intended use, classification, authorization, technical file and circulation number/permit if applicable.	Medical-device review before import or market release.	Importer, Regulatory and Legal.	Beauty claims cross into treatment claims; no device classification.	Review label, manual, brochure and website claims before purchase.
Labelling file	Original label, Vietnamese supplementary label, electrical specs, battery warnings, origin, manufacturer and responsible importer.	Market circulation and post-clearance/market inspection.	Importer, Brand and Compliance.	Missing Vietnamese, wrong origin or missing safety warning.	Review Decree 43/2017 and 111/2021 before arrival or warehouse release.

法律依据与专业政策矩阵

1. 需审核的法律文件

法律组	文件名称	发布机关	效力/时间	手续作用	重点条款/附件	审核说明
Cosmetics management	Circular 06/2011/TT-BYT and Circular 34/2025/TT-BYT	Ministry of Health	Circular 34/2025 effective 18 Aug 2025.	Applies when the set includes gel/serum/topical cosmetics.	Do not use cosmetic notification as proof for the device itself.	Review actual product file.
Medical devices	Decree 98/2021/ND-CP, Decree 07/2023/ND-CP, Circular 05/2022/TT-BYT	Government / MOH	Decree 98 effective 1 Jan 2022; Decree 07 effective 3 Mar 2023.	Review when the device has medical or therapeutic intended use.	Circulation conditions, classification and regulatory file.	Review intended use, claims and manual.
ICT / RF	Circular 02/2024/TT-BTTTT	Ministry of Information and Communications	Check effectiveness and list at import time.	Applies if wireless function and HS/product description fall under the list.	The circular applies only to listed HS and descriptions.	Review RF spec and module.
Product quality	Law 05/2007/QH12, Decree 132/2008/ND-CP, Decree 74/2018/ND-CP	National Assembly / Government	Decree 132 effective 1 Feb 2009; Decree 74 effective 1 Jul 2018.	Framework for Group 2 goods, quality inspection and conformity.	Review when goods fall under unsafe-product lists.	Do not apply generally without list confirmation.
Electrical safety	QCVN 4:2009/BKHCN and Amendment 1:2016 under Circular 21/2016/TT-BKHCN	MOST	Circular 21 effective 1 Feb 2017.	Review for electrical/electronic appliances within scope.	Not every beauty device automatically falls under QCVN 4.	Review model, power, voltage and purpose.
Goods labelling	Decree 43/2017/ND-CP, Decree 111/2021/ND-CP	Government	Decree 43 effective 1 Jun 2017; Decree 111 effective 15 Feb 2022.	Regulates labelling of imported and circulated goods.	Vietnamese label and mandatory information.	Review original label and supplementary label.
Lithium-battery transport	IATA DGR/BSR, IMDG Code and UN Manual of Tests and Criteria	IATA / IMO / UN	Updated periodically, especially for air transport.	Applies to devices with lithium batteries.	UN38.3, MSDS, Wh rating and packing instruction.	Review with DG specialist before booking.
Tariff, HS and VAT	Current import tariff, VAT schedule and FTA schedules	Ministry of Finance / Government	Changes by period.	Determines ordinary duty, MFN, VAT and FTA preference.	Do not finalize tax before final HS and origin are confirmed.	Check at declaration date.

2. 专业政策矩阵

货物情形	需对照文件	可能适用政策	主管机关/门户	触发条件
Standard beauty device without wireless/medical claim	HS, labelling, battery if any and electrical safety if listed.	Normal customs procedure plus labelling/battery review.	Customs and specialized authority if triggered.	Catalogue shows normal personal-care use.
Device with lithium battery	IATA/IMDG, UN38.3, MSDS and battery declaration.	Battery/DG transport review and package marking.	Forwarder, carrier, airline/warehouse.	Lithium battery, Wh rating, contained/packed with equipment.
Device with Wi‑Fi/Bluetooth/RF	Circular 29/2025/TT-BKHCN; Circular 02/2024/TT-BTTTT for pre-31 Dec 2025 comparison and relevant QCVN.	Possible ICT conformity certification/declaration.	MIC / VNTA / specialized portal if triggered.	Wireless module and listed HS/description.
Device with medical/therapeutic claims	Decree 98/2021, Decree 07/2023 and Circular 05/2022.	Possible medical-device classification and circulation requirements.	Ministry of Health / medical-device portal.	Treatment, diagnosis, rehabilitation or clinical claims.
Device sold with gel/serum/cosmetic product	Circular 06/2011 and 34/2025.	Cosmetic notification may be required for topical product.	Public service portal / health authority.	Topical cosmetic product included in the set.
Samples, demo, warranty or refurbished devices	Customs and relevant specialized policy.	Purpose-based import review; used-goods/warranty/temporary import may arise.	Customs and specialized authority if any.	Non-commercial, warranty, repaired or demo condition.

原文/官方来源

第34/2025/TT-BYT号通知第98/2021/ND-CP号法令第07/2023/ND-CP号法令第29/2025/TT-BKHCN号通知第43/2017/ND-CP号法令 IATA电池运输规则

处理时间、费用及风险成本

时间节点	需办理事项	可能费用	延误风险
T–21 to T–14 before ETA	Collect catalogue, datasheet, manual, label photos, battery spec, RF spec, marketing claims and C/O draft.	No state fee; translation/testing/consulting cost may arise.	HS, DG, ICT or medical-device route cannot be fixed before shipment.
T–14 to T–10	Confirm reference HS, C/O/FTA, label, battery status, wireless/medical/cosmetic-product triggers.	Depends on testing or certification if triggered.	C/O preference may be lost or commercial documents may need amendments.
T–10 to T–5	Start ICT/medical-device/cosmetic-notification file if triggered; lock battery/DG booking.	Cosmetic notification, if triggered, publicly shows 500,000 VND/item and 3–5 working days depending on dossier status.	Filing after ETA may cause storage or delivery delay.
ETA – customs declaration	File customs declaration, submit specialized documents if any and handle Green/Yellow/Red channel.	Customs/logistics costs by actual case.	Customs may query HS, claim, battery, catalogue, C/O and label.
Post-clearance / before market release	Apply supplementary label, retain files by model/shipment and complete any post-clearance obligations.	Label, warehouse, testing or certification costs if required.	Market inspection, post-clearance audit and traceability risk.

E2E实操流程

1. Review product nature before ETA

Identify whether the goods are normal beauty devices, electrical appliances, ICT/RF devices, medical devices, lithium-battery products or device + cosmetic combos.

2. Lock documents and technical files

Lock Invoice, Packing List, B/L/AWB, catalogue, datasheet, user manual, label photos, model/serial list, battery spec and C/O draft.

3. Determine specialized procedures

Separate customs, labelling, battery/DG, ICT, medical-device and cosmetic-notification layers if applicable.

4. File applications if triggered

Prepare cosmetic notification for topical products, ICT/medical-device file if listed, or lithium-battery/DG documents before booking.

5. Customs declaration and channel handling

Green channel is system-based, Yellow checks documents, Red checks documents and physical goods. Main query points: HS, model, battery, claims, C/O and catalogue.

6. Release, delivery and post-clearance obligations

Deliver to warehouse, apply supplementary label, retain files by model/shipment and prepare post-clearance explanation files.

常见问题

1. 电动美容设备是否需要办理化妆品公布？

Normally no, because the device itself is not a cosmetic product. If gel, serum or topical cosmetic products are sold together, those products must be reviewed separately.

2. 洁面仪或按摩仪是否需要进口许可证？

It depends on HS, battery, labelling, electrical safety, wireless function and claims. A normal non-wireless beauty device usually focuses on customs, labels, C/O and battery documents.

3. LED面罩或IPL脱毛仪可能被认定为医疗器械吗？

Yes, if the label/manual/website shows treatment, diagnosis, dermatology, rehabilitation or clinical use. Beauty-care claims must be separated from medical claims.

4. 带蓝牙/Wi‑Fi是否会触发ICT合格评定？

Only if the product has wireless function and its HS/product description falls under the current ICT Group 2 list. RF data and module specs are required.

5. 带锂电池走空运需要准备什么？

Battery spec, Wh rating, MSDS/SDS, UN38.3, battery configuration, packing instruction and carrier acceptance conditions.

6. 能否只凭“beauty device”确定HS编码？

No. HS is determined by principal function, structure, power source, technology, accessories and intended use.

7. C/O能否降低进口税？

Possibly, if the form, origin criteria, description, HS, quantity, direct transport and validity are compliant.

8. 样品或测试机是否与商业货物处理不同？

They may be different in purpose, value and explanation file, but specialized policy is not automatically waived.

9. 适配器或充电器是否需要单独归类？

It depends on set configuration and commercial documents. If imported separately, HS review may be required.

10. 通关后需要留存什么资料？

Customs declaration, commercial documents, C/O, catalogue, datasheet, labels, battery documents and any ICT/medical/cosmetic file if triggered.

最终结果及通关后义务

结果/输出	需完成义务
Customs declaration and clearance file	Keep with Invoice, Packing List, B/L/AWB, C/O and catalogue for post-clearance audit.
Specialized result/file if triggered	May include ICT, medical-device, cosmetic-notification or lithium-battery/DG documents.
Vietnamese label and market-release file	Must match product name, model, origin, electrical/battery specs, warnings and responsible importer.
Traceability file by model/shipment	Keep model list, serial list, photos, claims, manual and HS/policy explanation.

TGIMEX 解决方案

对于该类产品，企业应在ETA前同步审核物流、单证、海关、锂电池/DG、C/O及专业监管政策。重点不是单纯快速报关，而是到港前完整控制资料。

1. HS and policy review by model

Review catalogue, function, battery, RF, claims, accessories and import purpose to avoid wrong regulatory route.

2. C/O and landed-cost control

Check C/O form, origin criteria, HS on C/O, MFN/FTA duty, VAT and preference risk.

3. Lithium battery and transport booking

Check UN38.3, MSDS, Wh rating, battery configuration, package marking and carrier restrictions.

4. Labelling, claims and market file

Review original/supplementary label, claims, manual and safety warnings before market release.

5. Specialized-file preparation if triggered

Coordinate ICT, medical-device or cosmetic-notification file if the shipment has relevant triggers.

6. Customs, delivery and post-clearance file

Monitor ETA, pre-alert, declaration, channel handling, warehouse delivery and post-clearance records.

分阶段支持路径

支持阶段	重点工作	企业获得的输出
Before purchasing	Review model, claims, battery, RF function, accessories and supplier documents.	Supplier-data checklist and early policy-trigger warning.
Before ETD/ETA	Lock HS, C/O, SDS/MSDS, UN38.3, labels, catalogue and commercial documents.	Cross-checked file to reduce amendments and booking risk.
Arrival and declaration	Coordinate customs filing, channel handling, HS/model/battery/claim explanation and cargo release.	Clear workflow among Docs, Ops, Customs, Warehouse and importer.
Post-clearance	Retain files by model/shipment, check supplementary label and prepare audit file.	Complete record for market release and traceability.

电气－电子－IT设备

F&B

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家用产品

化妆品 – 个人护理

电气－电子－IT设备

F&B

机械设备

家用产品

化妆品－个人护理

电子产品 – 电子元器件 – ICT

机械 – 机械工程 – 工业设备

纺织 – 服装 – 鞋类 – 原辅料

木材 – 家具 – 木制品

农产品

水产品 – 动物源产品

食品饮料 – 加工食品 – 饮料

化学品 – 塑料 – 橡胶 – 原料

钢铁 – 铝 – 金属 – 建筑材料

项目货物 – 危险品 – 冷藏 – 超限货物

包装 – 纸张 – 印刷

陶瓷 – 手工艺品 – 石材 – 竹藤制品

药品 – 医疗器械 – 健康护理

化妆品 – 个人护理 – 家居护理

汽车 – 摩托车零部件 – 新能源汽车

电动/电池/科技类美容设备进口手续指南