Taiwan FDA registration 42b7b40aeae8bb7de554335aeada6330

Vitex biochemical products barbiturate reagent

TW: 維特司生化產品巴比妥酸鹽試劑

Taiwan·Risk Class 2·ORTHO-CLINICAL DIAGNOSTICS, INC.;; ORTHO-CLINICAL DIAGNOSTICS, INC·Registered May 04, 2009 – May 04, 2024Expired

Registration details

Analysis ID: 42b7b40aeae8bb7de554335aeada6330
Customs Code: DHA00602000304

Company information

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

Product details

Intended Use: Semi-quantitative or qualitative determination of barbiturates (BARBs) in human urine.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.3150 Barbiturate salt testing system
Import Information: import

Dates and status

Registration Date: May 04, 2009
Expiry Date: May 04, 2024

About this record

Access comprehensive regulatory information for Vitex biochemical products barbiturate reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 42b7b40aeae8bb7de554335aeada6330 and manufactured by ORTHO-CLINICAL DIAGNOSTICS, INC.;; ORTHO-CLINICAL DIAGNOSTICS, INC. The authorized representative in Taiwan is DKSH TAIWAN LTD..

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