カナダ掲示板 (金融・税金) - No.255926

コードは9019.10.00.20かな？

関税はざっくり2割くらいじゃないかな、私も専門家じゃないので正確じゃないけど。
合計金額60ドル以上で課税される可能性あります。

あと、その高周波治療器はカナダの電圧(日本と違う）対応ですか？
対応じゃない場合、危険かもだし、故障の際も無償修理適応外になるんじゃないかな。
個人的には電化製品(パソコンなど海外で使える前提のもの以外）のギフトはおススメしません。

通常ギフトとして送る場合、４～５００ドル以下なら申請金額に対して消費税のHSTだけです。

同じ人/住所に＄６０以下の物を何度も送ると関税云々よりも別の疑いを抱かれ、念入りに調べられますよ。

中身を記載する際、マッサージ器でOKでは、誰が見ても医療機器と思える物でなければ大丈夫です。疑いがあれば受取際（郵便局などで）に中身を確認されるので申請書類と違っていると問題ですよ。

Gifts

For an item to qualify as a "gift", a friend or relative must send it to you personally and include a card or other notice indicating that it is a gift.

If you receive an imported gift by mail that is worth CAN$60 or less, you will not have to pay duty and/or tax on it.
If the gift is worth more than CAN$60, you will have to pay any applicable duty and/or taxes on any amount over CAN$60.

For example, if a relative sends you a gift worth CAN$200, you must pay any applicable duty, GST or HST and/or PST on CAN$140.
Items that do not qualify for the CAN$60 gift exemption include the following:

tobacco;
alcoholic beverages;
advertising material; and
items sent by a business.

As well, the CAN$60 gift exemption cannot be combined with the CAN$20 exemption that is available on most items valued at CAN$20 or less.

https://www.cbsa-asfc.gc.ca/import/courier/menu-eng.html

Importations Into Canada

The gift exemption for eligible gifts imported into Canada is CAD$60 or less, per gift, even if a single gift has more than one recipient (e.g., gift to a family). Each gift in the shipment must be clearly identified as one gift. If the gift is worth more than CAD$60, the amount over CAD$60 is subject to duties and taxes (e.g., if a relative sends you a gift worth CAD$200, you must pay any applicable duty plus the GST, HST or QST on CAD$140).

The CAD$60 exemption that's available for gifts cannot be combined with the general CAD$20 exemption that's available on all items.

https://www.fedex.com/en-ca/shipping-services/international/regulatory/tips-for-gift-shipments.html

>誰が見ても医療機器と思える物でなければ大丈夫です。

医療機器なら関税ゼロなんじゃないの？

法に触れるとやっかいだよ。厚生省所管だし。

変な薬物でもないのに法には触れないだろｗ
マッサージ器ってそんなに危ない物かよ。

例だけどね、かなり厳しいんだよ。

家庭用マッサージ器は管理医療機器に該当します。医薬品医療機器等法の規定により、販売を行う場合は事前に販売業の届出が必要です。
たとえ1回のみの販売であっても医薬品医療機器等法に違反する恐れがあります。

それ販売な。しかも日本な。

例だからね、だけど所管がうるさい官庁とか関わらない方がいいよ。

Who can import
An importer is any person in Canada, other than the manufacturer of a medical device, who is responsible for the medical device coming into Canada. Anyone who imports a medical device into Canada must also meet all applicable requirements of the FDA and associated Regulations. Some requirements include the following:

Class I device: The importer must have a valid Medical Device Establishment Licence (MDEL) with the activity of import, unless exempted
Class II, III or IV device: The device must be licensed by having a Medical Device Licence (MDL) and the importer must have a valid MDEL with the activity of import, unless exempted
All medical device classes: The importer must ensure that the company from whom they import (foreign distributor) has an MDEL that includes the appropriate licensable activities, unless exempted

Exemptions
Importers are exempt if they are a:

retailer/company that only sells directly to the end user for their own personal use
health care facility
Class I medical device manufacturer that imports only Class I medical devices through someone else who has an MDEL
manufacturer of Class II, III or IV medical devices that only sells:
medical devices for which they hold a valid licence or
custom-made medical devices, medical devices for special access or medical devices for investigational testing involving humans for which a valid authorization has been issued
person who only imports or sells veterinary medical devices
Dispenser (member of a recognized professional association who can make or adapt a medical device for a particular patient in accordance with a professional's written direction in order to meet the specific requirements of a patient)
person who only imports or sells custom-made medical devices (manufactured only for a particular patient in accordance with a professional's written direction), medical devices for special access or medical devices for investigational testing involving humans, for which a valid authorization has been issued