Taiwan FDA registration afdcb465f8333435d69225755c3713f2

Vitex biochemical products tabletop isomerase tube solution

TW: 維特司生化產品桌上型同功異構酶品管液

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

Registration details

Analysis ID: afdcb465f8333435d69225755c3713f2
Customs Code: DHA00601647800

Company information

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

Product details

Intended Use: It is used to monitor performance on the Waters desktop biochemical system.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1660 Quality control materials (analytical and non-analytical)
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 products tabletop isomerase tube solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number afdcb465f8333435d69225755c3713f2 and manufactured by ORTHO-CLINICAL DIAGNOSTICS, INC.;; ORTHO-CLINICAL DIAGNOSTICS, INC. The authorized representative in Taiwan is DKSH TAIWAN LTD..

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