Taiwan FDA registration 6febc520b8d31aeb5a0bad796be43690

Vitex biochemical tabletop isomerase correction group

TW: 維特司生化產品桌上型同功異構酶校正組

Taiwan·Risk Class 2·ORTHO-CLINICAL DIAGNOSTICS, INC.;; ORTHO-CLINICAL DIAGNOSTICS, INC·Registered Apr 26, 2006 – Apr 26, 2016Cancelled

Registration details

Analysis ID: 6febc520b8d31aeb5a0bad796be43690
Customs Code: DHA00601647708

Company information

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

Product details

Intended Use: CKMB for calibration of Vites desktop biochemical systems.
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: Apr 26, 2006
Expiry Date: Apr 26, 2016
Cancellation Date: Aug 14, 2018

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for Vitex biochemical tabletop isomerase correction group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6febc520b8d31aeb5a0bad796be43690 and manufactured by ORTHO-CLINICAL DIAGNOSTICS, INC.;; ORTHO-CLINICAL DIAGNOSTICS, INC. The authorized representative in Taiwan is DKSH TAIWAN LTD..

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