Taiwan FDA registration b4b1f67f763a9b191dd155f155d9c678

Vetex Biochemical Products No. 32 Correction Solution

TW: 維特司生化產品32號校正液

Taiwan·Risk Class 2·ORTHO-CLINICAL DIAGNOSTICS, INC.·Registered Jan 18, 2021 – Jan 18, 2026Expired

Registration details

Analysis ID: b4b1f67f763a9b191dd155f155d9c678
Customs Code: DHA05603419700

Company information

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

Product details

Intended Use: This product is an in vitro diagnostic reagent for the calibration of VITORS 250/350/5, 1 FS/4600/XT 3400 automatic biochemistry analyzer and VITROS 5600/XT 7600 automatic biochemical immunoassay analyzer for the quantitative detection of sodium, chloride, potassium and carbonate (ECO2).
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1150 Calibrated Products
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: Jan 18, 2021
Expiry Date: Jan 18, 2026

About this record

Access comprehensive regulatory information for Vetex Biochemical Products No. 32 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 b4b1f67f763a9b191dd155f155d9c678 and manufactured by ORTHO-CLINICAL DIAGNOSTICS, INC.. The authorized representative in Taiwan is DKSH TAIWAN LTD..

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