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"Nippon Medical" medium frequency vector interference wave therapy instrument - Taiwan Registration 6178610ea52a3d2f6760060e52d7ee5c

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.

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6178610ea52a3d2f6760060e52d7ee5c
Registration Details
Taiwan FDA Registration: 6178610ea52a3d2f6760060e52d7ee5c
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Device Details

"Nippon Medical" medium frequency vector interference wave therapy instrument
TW: โ€œๆ—ฅๆœฌ้†ซ็™‚โ€ไธญ้ ปๅ‘้‡ๅนฒๆ“พๆณขๆฒป็™‚ๅ„€
Risk Class 2
Cancelled

Registration Details

6178610ea52a3d2f6760060e52d7ee5c

DHA00602329009

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

o Physical Medical Sciences

O.5850 5850.

import

Dates and Status

Mar 03, 2012

Mar 03, 2022

Apr 12, 2024

Cancellation Information

Logged out

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