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"Roche" interstitial transformation factor nucleic acid probe (unsterilized) - Taiwan Registration 5e2d333d675ce67d3a57df78823f0e3e

Access comprehensive regulatory information for "Roche" interstitial transformation factor nucleic acid 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 5e2d333d675ce67d3a57df78823f0e3e and manufactured by ROCHE DIAGNOSTICS GMBH;; VENTANA MEDICAL SYSTEMS, INC.. The authorized representative in Taiwan is ROCHE DIAGNOSTICS LTD..

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5e2d333d675ce67d3a57df78823f0e3e
Registration Details
Taiwan FDA Registration: 5e2d333d675ce67d3a57df78823f0e3e
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Device Details

"Roche" interstitial transformation factor nucleic acid probe (unsterilized)
TW: "็พ…ๆฐ"ไธŠ็šฎ็ดฐ่ƒž้–“่ณช่ฝ‰ๅŒ–ๅ› ๅญๆ ธ้…ธๆŽข้‡(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

5e2d333d675ce67d3a57df78823f0e3e

DHA04401012200

Company Information

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

import

Dates and Status

Mar 31, 2011

Mar 31, 2016

May 28, 2018

Cancellation Information

Logged out

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