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"Chaoyang" digital low-frequency therapy device - Taiwan Registration 3f8aabd5bf313a73ed8aec409d96aaf5

Access comprehensive regulatory information for "Chaoyang" digital 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 3f8aabd5bf313a73ed8aec409d96aaf5 and manufactured by Chaoyang Plastic Factory Co., Ltd. The authorized representative in Taiwan is Chaoyang Plastic Factory Co., Ltd.

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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3f8aabd5bf313a73ed8aec409d96aaf5
Registration Details
Taiwan FDA Registration: 3f8aabd5bf313a73ed8aec409d96aaf5
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Device Details

"Chaoyang" digital low-frequency therapy device
TW: "ๆœๆš" ๆ•ธไฝไฝŽ้€ฑๆณขๆฒป็™‚ๅ™จ
Risk Class 2

Registration Details

3f8aabd5bf313a73ed8aec409d96aaf5

DHY00500141302

Company Information

Taiwan, Province of China

Product Details

Relieves shoulder pain and peripheral nerve paralysis, and promotes local blood circulation.

K Neuroscience

Domestic

Dates and Status

Aug 12, 2005

Aug 12, 2025