Taiwan FDA registration c55cc2ff3a91f91c8bed752dccf436da
Melaleuc Low Frequency Therapy Device
TW: 美樂樂低周波治療器
Taiwan·Risk Class 2·Fengmao Technology Co., Ltd. third factory·Registered Dec 10, 2008 – Dec 10, 2013CancelledRegistration details
- Analysis ID
- c55cc2ff3a91f91c8bed752dccf436da
- Customs Code
- DHY00500256807
Company information
- Manufacturer
- Fengmao Technology Co., Ltd. third factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- A-CLEVER TECHNOLOGY CO., LTD.
Product details
- Intended Use
- Relieves shoulder soreness, peripheral nerve paralysis, and promotes local blood circulation.
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.5890 Transcutaneous electrical nerve stimulator for pain relief
- Import Information
- Domestic
Dates and status
- Registration Date
- Dec 10, 2008
- Expiry Date
- Dec 10, 2013
- Cancellation Date
- Jun 02, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Melaleuc Low Frequency 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 c55cc2ff3a91f91c8bed752dccf436da and manufactured by Fengmao Technology Co., Ltd. third factory. The authorized representative in Taiwan is A-CLEVER TECHNOLOGY CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices