Taiwan FDA registration d6fd5b4b26263095d75ceff91d749689

Vitex Biochemical Products Correction Group No. 26

TW: 維特司生化產品校正組 26 號
Taiwan flagTaiwan·Risk Class 2·ORTHO-CLINICAL DIAGNOSTICS, INC.;; ORTHO-CLINICAL DIAGNOSTICS, INC·Registered May 14, 2009 – May 14, 2029Active
Registration details
Analysis ID
d6fd5b4b26263095d75ceff91d749689
Customs Code
DHA00602001205
Company information
Manufacturer Country
United States
Authorized Representative
DKSH TAIWAN LTD.
Product details
Intended Use
The VITROS Biochemical Calibration Group No. 26 is used to calibrate the VITROS 5, 1 FS chemical analyzer for the qualitative or semi-quantitative determination of the content of drugs of abuse in humans.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1150 Calibrated Products
Import Information
import
Dates and status
Registration Date
May 14, 2009
Expiry Date
May 14, 2029
About this record

Access comprehensive regulatory information for Vitex Biochemical Products Correction Group No. 26 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d6fd5b4b26263095d75ceff91d749689 and manufactured by ORTHO-CLINICAL DIAGNOSTICS, INC.;; ORTHO-CLINICAL DIAGNOSTICS, INC. The authorized representative in Taiwan is DKSH TAIWAN LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free DatabasePowered by Pure Global AI89,000+ Devices