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Roche Real-Time Fluorescent EBV Quantitative Test Kit (Unsterilized) - Taiwan Registration b860c9b88dca47dcfdb3c54c93ece6b3

Access comprehensive regulatory information for Roche Real-Time Fluorescent EBV Quantitative Test Kit (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b860c9b88dca47dcfdb3c54c93ece6b3 and manufactured by CEPHEID AB. 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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Registration Details
Taiwan FDA Registration: b860c9b88dca47dcfdb3c54c93ece6b3
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Device Details

Roche Real-Time Fluorescent EBV Quantitative Test Kit (Unsterilized)
TW: โ€œ็พ…ๆฐโ€ๅณๆ™‚่žขๅ…‰EBVๅฎš้‡ๆชข้ฉ—่ฉฆๅŠ‘ๅฅ—็ต„(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

b860c9b88dca47dcfdb3c54c93ece6b3

DHA04400905103

Company Information

Sweden

Product Details

Limited to the first level identification range of "Epstein-Barr virus serum reagent (C.3235)" of the Measures for the Administration of Medical Devices.

C Immunology and microbiology

C.3235 EB็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Aug 05, 2010

Aug 05, 2015

May 28, 2018

Cancellation Information

Logged out

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