Low frequency therapy device
Taiwan·DAINICHI KOUGYOU GIKEN CO., LTD.·Registered Aug 05, 1998 – Aug 05, 2003Cancelled- Analysis ID
- 787b592c3240e9e2842beacdf2dc7804
- Customs Code
- DHA00600879704
- Manufacturer
- DAINICHI KOUGYOU GIKEN CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- PEKO INCORPORATION
- Product Type (Level 1)
- 1805 Low Frequency Therapy Device
- Import Information
- import
- Registration Date
- Aug 05, 1998
- Expiry Date
- Aug 05, 2003
- Cancellation Date
- Jul 11, 2003
- Status
- Logged out
- Reason
- 自請註銷
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Access comprehensive regulatory information for Low frequency therapy device in Taiwan's medical device market through Pure Global AI's free database. is registered under number 787b592c3240e9e2842beacdf2dc7804 and manufactured by DAINICHI KOUGYOU GIKEN CO., LTD.. The authorized representative in Taiwan is PEKO INCORPORATION.
This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including SHIAN JIA MEEI ENTERPRISE CO., LTD., MINATO MEDICAL SCIENCE CO. LTD. NISHIKI FACILITY, and 5 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.