Taiwan FDA registration a99ae9c31827e238d2544aed2d0d261e
"Meriti" muscle stimulator
TW: “美利帝”肌肉刺激器
Taiwan·Risk Class 2·Verity Medical Ltd.·Registered Sep 20, 2019 – Sep 20, 2029ActiveRegistration details
- Analysis ID
- a99ae9c31827e238d2544aed2d0d261e
- Customs Code
- DHA05603288304
Company information
- Manufacturer
- Verity Medical Ltd.
- Manufacturer Country
- Ireland
- Authorized Representative
- CONTINUOUS INSTRUMENT CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K 神經科學;; H 胃腸病科學及泌尿科學;; O 物理醫學科學
- Product Type (Level 2)
- H.5320 Non-implantable electronic urination home-made device;; O.5850 Powered Muscle Stimulator;; K.5890 Transcutaneous electrical nerve stimulator for pain relief
- Import Information
- import
Dates and status
- Registration Date
- Sep 20, 2019
- Expiry Date
- Sep 20, 2029
About this record
Access comprehensive regulatory information for "Meriti" muscle stimulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a99ae9c31827e238d2544aed2d0d261e and manufactured by Verity Medical Ltd.. The authorized representative in Taiwan is CONTINUOUS INSTRUMENT CO., LTD..
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