Taiwan FDA registration c8cf5de8a746a248448f7be52c0aa261

Vites biochemical products opioids

TW: 維特司生化產品鴉片類試劑

Taiwan·Risk Class 2·ORTHO-CLINICAL DIAGNOSTICS, INC.;; ORTHO-CLINICAL DIAGNOSTICS, INC·Registered May 04, 2009 – May 04, 2019Cancelled

Registration details

Analysis ID: c8cf5de8a746a248448f7be52c0aa261
Customs Code: DHA00602000406

Company information

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

Product details

Intended Use: 半定量或定性測定人類尿液中鴨片類 (OP) 的含量.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.3650 Opium testing system
Import Information: import

Dates and status

Registration Date: May 04, 2009
Expiry Date: May 04, 2019
Cancellation Date: Feb 19, 2019

Cancellation information

Status: Logged out
Reason: 自請註銷

About this record

Access comprehensive regulatory information for Vites biochemical products opioids in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c8cf5de8a746a248448f7be52c0aa261 and manufactured by ORTHO-CLINICAL DIAGNOSTICS, INC.;; ORTHO-CLINICAL DIAGNOSTICS, INC. The authorized representative in Taiwan is DKSH TAIWAN LTD..

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