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"Meridian" sleep physiology detector - Taiwan Registration 78f08e1b848e864c8002789ae7b8d93e

Access comprehensive regulatory information for "Meridian" sleep physiology detector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 78f08e1b848e864c8002789ae7b8d93e and manufactured by Meridian Power Medical Co., Ltd. Xizhi Factory. The authorized representative in Taiwan is Meridian Power Medical 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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78f08e1b848e864c8002789ae7b8d93e
Registration Details
Taiwan FDA Registration: 78f08e1b848e864c8002789ae7b8d93e
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Device Details

"Meridian" sleep physiology detector
TW: โ€œ็ถ“็ตกโ€็ก็œ ็”Ÿ็†ๆชขๆธฌๅ™จ
Risk Class 2
Cancelled

Registration Details

78f08e1b848e864c8002789ae7b8d93e

DHY00500222503

Company Information

Taiwan, Province of China

Product Details

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

D Anesthesiology

D.2375 Respiratory frequency monitor

Domestic

Dates and Status

Jun 20, 2007

Jun 20, 2012

Apr 14, 2014

Cancellation Information

Logged out

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