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Low frequency therapy device - Taiwan Registration 787b592c3240e9e2842beacdf2dc7804

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.

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787b592c3240e9e2842beacdf2dc7804
Registration Details
Taiwan FDA Registration: 787b592c3240e9e2842beacdf2dc7804
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Device Details

Low frequency therapy device
TW: ไฝŽ้€ฑๆณขๆฒป็™‚ๅ„€
Cancelled

Registration Details

787b592c3240e9e2842beacdf2dc7804

DHA00600879704

Company Information

Product Details

1805 Low Frequency Therapy Device

import

Dates and Status

Aug 05, 1998

Aug 05, 2003

Jul 11, 2003

Cancellation Information

Logged out

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