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"Roche" negative quality tube probe (unsterilized) - Taiwan Registration 301ab772b06f224b59c8c95cd19d6c22

Access comprehensive regulatory information for "Roche" negative quality tube probe (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 301ab772b06f224b59c8c95cd19d6c22 and manufactured by VENTANA MEDICAL SYSTEMS, INC.. The authorized representative in Taiwan is ROCHE DIAGNOSTICS 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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301ab772b06f224b59c8c95cd19d6c22
Registration Details
Taiwan FDA Registration: 301ab772b06f224b59c8c95cd19d6c22
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Device Details

"Roche" negative quality tube probe (unsterilized)
TW: "็พ…ๆฐ" ้™ฐๆ€งๅ“็ฎกๆŽข้‡(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

301ab772b06f224b59c8c95cd19d6c22

DHA09402300905

Company Information

United States

Product Details

Limited to the classification and grading management of medical equipment, quality control materials (analytical and non-analytical) (A.1660) the first level identification range.

A Clinical chemistry and clinical toxicology

A.1660 Quality control materials (analytical and non-analytical)

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Jan 11, 2023

Jan 11, 2028