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"Draida" clinical sample (unsterilized) - Taiwan Registration f7cbd379b5fc892d6c7b98c1ceb9dde1

Access comprehensive regulatory information for "Draida" clinical sample (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f7cbd379b5fc892d6c7b98c1ceb9dde1 and manufactured by DETEKT TECHNOLOGY INC.. The authorized representative in Taiwan is DETEKT TECHNOLOGY INC..

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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f7cbd379b5fc892d6c7b98c1ceb9dde1
Registration Details
Taiwan FDA Registration: f7cbd379b5fc892d6c7b98c1ceb9dde1
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Device Details

"Draida" clinical sample (unsterilized)
TW: "ๅพท่Šฎ้”" ่‡จๅบŠ็”จๆจฃๆฟ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

f7cbd379b5fc892d6c7b98c1ceb9dde1

Company Information

Taiwan, Province of China

Product Details

Limited to the classification and grading management measures of medical equipment "Clinical Use Model (N.4800) First Level Identification Range".

N Orthopedics

N.4800 Sample plate for clinical use

QMS/QSD;; ๅœ‹็”ข

Dates and Status

Mar 23, 2018

Mar 23, 2028