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"Silka" Thopras low-frequency therapy device - Taiwan Registration 17ff5175c3c179a83214be12884a6b0a

Access comprehensive regulatory information for "Silka" Thopras low-frequency therapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 17ff5175c3c179a83214be12884a6b0a and manufactured by CELCOM, INC.. The authorized representative in Taiwan is GOOD LINE INCORPORATION.

This page provides complete technical specifications, regulatory compliance details. 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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17ff5175c3c179a83214be12884a6b0a
Registration Details
Taiwan FDA Registration: 17ff5175c3c179a83214be12884a6b0a
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Device Details

"Silka" Thopras low-frequency therapy device
TW: โ€œๆ€็ˆพๅกโ€้€ๆ™ฎๆ‹‰ไฝŽ้ ปๆฒป็™‚ๅ™จ
Risk Class 2
Cancelled

Registration Details

17ff5175c3c179a83214be12884a6b0a

DHA00601855002

Company Information

Japan

Product Details

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

K Neuroscience

K.5890 Transcutaneous electrical nerve stimulator for pain relief

import

Dates and Status

Jan 18, 2008

Jan 18, 2013

Jun 03, 2015

Cancellation Information

Logged out

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