Taiwan FDA registration 71d95528e95dae73b9db103a40f556aa
Kawasaki potential therapy device
TW: 川崎電位治療器
Taiwan·Risk Class 2·Morita Kogyo Co., Ltd. Minakami Factory·Registered Jul 26, 2006 – Aug 30, 2010CancelledRegistration details
- Analysis ID
- 71d95528e95dae73b9db103a40f556aa
- Customs Code
- DHY00500188807
Company information
- Manufacturer
- Morita Kogyo Co., Ltd. Minakami Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Morita Kogyo Co., Ltd. Minakami Factory
Product details
- Intended Use
- Relieves stiff shoulders, headaches, chronic constipation.
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.0001 靜電器(電位治療器)
- Import Information
- Domestic
Dates and status
- Registration Date
- Jul 26, 2006
- Expiry Date
- Aug 30, 2010
- Cancellation Date
- Oct 30, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Kawasaki potential therapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 71d95528e95dae73b9db103a40f556aa and manufactured by Morita Kogyo Co., Ltd. Minakami Factory. The authorized representative in Taiwan is Morita Kogyo Co., Ltd. Minakami Factory.
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