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Vitex Biochemical Products Therapeutic Quality Assurance Fluids I, II and III - Taiwan Registration 7bb960a6926719416124cd7f72e2bb8b

Access comprehensive regulatory information for Vitex Biochemical Products Therapeutic Quality Assurance Fluids I, II and III in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7bb960a6926719416124cd7f72e2bb8b and manufactured by ORTHO-CLINICAL DIAGNOSTICS, INC. The authorized representative in Taiwan is DKSH TAIWAN LTD..

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7bb960a6926719416124cd7f72e2bb8b
Registration Details
Taiwan FDA Registration: 7bb960a6926719416124cd7f72e2bb8b
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Device Details

Vitex Biochemical Products Therapeutic Quality Assurance Fluids I, II and III
TW: ็ถญ็‰นๅธ็”ŸๅŒ–็”ขๅ“ๆฒป็™‚ๆ€ง่—ฅ็‰ฉ็›ฃๆŽงๅ“่ณช็ขบ่ชๆถฒ I,II ๅ’Œ III
Risk Class 2

Registration Details

7bb960a6926719416124cd7f72e2bb8b

DHA00601236006

Company Information

United States

Product Details

Vetex Biochemical Products Therapeutic Substance Monitoring Quality Confirmation Solution is used to monitor the performance of Vitex Biochemical Systems.

A Clinical chemistry and clinical toxicology

import

Dates and Status

Sep 14, 2005

Sep 14, 2025