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TERC/Chr3cen probe (unsterilized) - Taiwan Registration c234b0fa4a31c7ddc53911a906fcbc52

Access comprehensive regulatory information for TERC/Chr3cen 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 c234b0fa4a31c7ddc53911a906fcbc52 and manufactured by PLEXBIO CO., LTD.. The authorized representative in Taiwan is PLEXBIO 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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c234b0fa4a31c7ddc53911a906fcbc52
Registration Details
Taiwan FDA Registration: c234b0fa4a31c7ddc53911a906fcbc52
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Device Details

TERC/Chr3cen probe (unsterilized)
TW: โ€œๅš้Œธโ€TERC/Chr3cenๆŽข้‡ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

c234b0fa4a31c7ddc53911a906fcbc52

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of immunopathological histochemical reagents and kits (B.1860) of the Measures for the Administration of Medical Devices.

B Hematology, pathology, and genetics

B.1860 Immunopathological histochemistry reagents and kits

Domestic

Dates and Status

Jan 26, 2015

Jan 26, 2020

Dec 05, 2017

Cancellation Information

Logged out

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