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Vitex Biochemical FS IV Dilution Box (Unsterilized) - Taiwan Registration 52e38772ae7139c0a3cb9a35edaf1222

Access comprehensive regulatory information for Vitex Biochemical FS IV Dilution Box (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 52e38772ae7139c0a3cb9a35edaf1222 and manufactured by ORTHO-CLINICAL DIAGNOSTICS, INC.;; ORTHO-CLINICAL DIAGNOSTICS, INC. The authorized representative in Taiwan is DKSH TAIWAN LTD..

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52e38772ae7139c0a3cb9a35edaf1222
Registration Details
Taiwan FDA Registration: 52e38772ae7139c0a3cb9a35edaf1222
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Device Details

Vitex Biochemical FS IV Dilution Box (Unsterilized)
TW: ็ถญ็‰นๅธ็”ŸๅŒ–็”ขๅ“FSๅ››่™Ÿ็จ€้‡‹็›’(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

52e38772ae7139c0a3cb9a35edaf1222

DHA04400586401

Company Information

Product Details

Limited to the first level identification scope of "General Purpose Reaction Reagents (B.4010)" under the Measures for the Administration of Medical Devices.

B Hematology, pathology, and genetics

B.4010 Reaction Reagents for General Purposes

import

Dates and Status

May 18, 2007

May 18, 2017

Dec 13, 2019

Cancellation Information

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