Taiwan FDA registration 6e5a2aaba88b9a6cfc9a56e0a8b484d0
“Shian Jia Meei” Transcutaneous Electrical Nerve Stimulator
TW: “仙佳美”低週波治療器
Taiwan·Risk Class 2·MD·SHIAN JIA MEEI ENTERPRISE CO., LTD.·Registered May 01, 2015 – Sep 30, 2019CancelledRegistration details
- Analysis ID
- 6e5a2aaba88b9a6cfc9a56e0a8b484d0
- License Form
- Ministry of Health Medical Device Manufacturing No. 004861
Company information
- Manufacturer
- SHIAN JIA MEEI ENTERPRISE CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SHIAN JIA MEEI ENTERPRISE CO., LTD.
Product details
- Product Type (Level 1)
- K Devices for neuroscience
- Product Type (Level 2)
- K5890 Transcutaneous electrical nerve stimulator for pain relief
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- May 01, 2015
- Expiry Date
- Sep 30, 2019
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for “Shian Jia Meei” Transcutaneous Electrical Nerve Stimulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6e5a2aaba88b9a6cfc9a56e0a8b484d0 and manufactured by SHIAN JIA MEEI ENTERPRISE CO., LTD.. The authorized representative in Taiwan is SHIAN JIA MEEI ENTERPRISE CO., LTD..
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