Taiwan FDA registration 52e38772ae7139c0a3cb9a35edaf1222

Vitex Biochemical FS IV Dilution Box (Unsterilized)

TW: 維特司生化產品FS四號稀釋盒(未滅菌)

Taiwan·Risk Class 1·ORTHO-CLINICAL DIAGNOSTICS, INC.;; ORTHO-CLINICAL DIAGNOSTICS, INC·Registered May 18, 2007 – May 18, 2017Cancelled

Registration details

Analysis ID: 52e38772ae7139c0a3cb9a35edaf1222
Customs Code: DHA04400586401

Company information

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

Product details

Intended Use: Limited to the first level identification scope of "General Purpose Reaction Reagents (B.4010)" under the Measures for the Administration of Medical Devices.
Product Type (Level 1): B Hematology, pathology, and genetics
Product Type (Level 2): B.4010 Reaction Reagents for General Purposes
Import Information: import

Dates and status

Registration Date: May 18, 2007
Expiry Date: May 18, 2017
Cancellation Date: Dec 13, 2019

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for Vitex Biochemical FS IV Dilution Box (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 52e38772ae7139c0a3cb9a35edaf1222 and manufactured by ORTHO-CLINICAL DIAGNOSTICS, INC.;; ORTHO-CLINICAL DIAGNOSTICS, INC. The authorized representative in Taiwan is DKSH TAIWAN LTD..

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