"Nippon Medical" medium frequency vector interference wave therapy instrument
Taiwan·Risk Class 2·NIHON MEDIX CO., LTD. KASHIWA FACTORY·Registered Mar 03, 2012 – Mar 03, 2022Cancelled- Analysis ID
- 6178610ea52a3d2f6760060e52d7ee5c
- Customs Code
- DHA00602329009
- Manufacturer
- NIHON MEDIX CO., LTD. KASHIWA FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- CROWNMED ENTERPRISE CO., LTD.
- 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
- Registration Date
- Mar 03, 2012
- Expiry Date
- Mar 03, 2022
- Cancellation Date
- Apr 12, 2024
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for "Nippon Medical" medium frequency 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 6178610ea52a3d2f6760060e52d7ee5c and manufactured by NIHON MEDIX CO., LTD. KASHIWA FACTORY. The authorized representative in Taiwan is CROWNMED ENTERPRISE CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including NIHON MEDIX CO., LTD. KASHIWA FACTORY, and 1 recent registrations in the same category. 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.