Taiwan FDA registration cb40695156783fe26f1c9fccfa5c5b32

"Nippon Medical" medium frequency vector interference wave therapy instrument

TW: "日本醫療"中頻向量干擾波治療儀
Taiwan flagTaiwan·Risk Class 2·NIHON MEDIX CO., LTD. KASHIWA FACTORY·Registered Apr 18, 2006 – Apr 18, 2016Cancelled
Registration details
Analysis ID
cb40695156783fe26f1c9fccfa5c5b32
Customs Code
DHA00601431205
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
Import Information
import
Dates and status
Registration Date
Apr 18, 2006
Expiry Date
Apr 18, 2016
Cancellation Date
Aug 09, 2018
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

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 cb40695156783fe26f1c9fccfa5c5b32 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.

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