Taiwan FDA registration 0484a84a4103ca08c99c57f86cd821ac

Vitex Biochemical Products No. 5 Correction Solution

TW: 維特司生化產品5號校正液

Taiwan·Risk Class 2·ORTHO-CLINICAL DIAGNOSTICS, INC·Registered Sep 19, 2005 – Sep 19, 2025Expired

Registration details

Analysis ID: 0484a84a4103ca08c99c57f86cd821ac
Customs Code: DHA00601241801

Company information

Manufacturer: ORTHO-CLINICAL DIAGNOSTICS, INC
Manufacturer Country: United States
Authorized Representative: DKSH TAIWAN LTD.

Product details

Intended Use: Calibration of the Vitex biochemical system as a quantitative measurement of ammonia and protein. The following blank change performance (new applicable models) is: For in vitro diagnostic use only. This product is used to calibrate the Vitex biochemical system as a quantitative measurement of ammonia and protein. This product is required for use with the Vitex 350/5,1 FS/4600/XT3400 chemical analyzer and the Vitex 5600/XT7600 biochemical immunoassay analyzer. The following blanks
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Import Information: import

Dates and status

Registration Date: Sep 19, 2005
Expiry Date: Sep 19, 2025

About this record

Access comprehensive regulatory information for Vitex Biochemical Products No. 5 Correction Solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0484a84a4103ca08c99c57f86cd821ac and manufactured by ORTHO-CLINICAL DIAGNOSTICS, INC. The authorized representative in Taiwan is DKSH TAIWAN LTD..

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