Taiwan FDA registration 2b3f7eb04696e3c64b3701e253e26534
"Japanese Medical" vector interference wave therapy instrument
TW: “日本醫療”向量干擾波治療儀
Taiwan·Risk Class 2·Nihon Medix Co., Ltd. Kashiwa Factory;; DIGI I's Ltd.·Registered Jul 02, 2014 – Jul 02, 2029ActiveRegistration details
- Analysis ID
- 2b3f7eb04696e3c64b3701e253e26534
- Customs Code
- DHA05602638107
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- CROWNMED ENTERPRISE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.5850 5850.
- Import Information
- import
Dates and status
- Registration Date
- Jul 02, 2014
- Expiry Date
- Jul 02, 2029
About this record
Access comprehensive regulatory information for "Japanese Medical" vector interference wave therapy instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2b3f7eb04696e3c64b3701e253e26534 and manufactured by Nihon Medix Co., Ltd. Kashiwa Factory;; DIGI I's Ltd.. The authorized representative in Taiwan is CROWNMED ENTERPRISE CO., LTD..
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