Taiwan FDA registration accc5fb16541a334b7f929fe36d8989a

Vitex biochemical products α1 antitrypsin per reagent

TW: 維特司生化產品α1抗胰蛋白每試劑

Taiwan·Risk Class 2·ORTHO-CLINICAL DIAGNOSTICS, INC.;; ORTHO-CLINICAL DIAGNOSTICS, INC·Registered Aug 31, 2006 – Aug 31, 2016Cancelled

Registration details

Analysis ID: accc5fb16541a334b7f929fe36d8989a
Customs Code: DHA00601730204

Company information

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

Product details

Intended Use: Quantitatively measure the concentration of α1 antitryptin in serum.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.5130 α-1-抗胰蛋白免疫試驗系統
Import Information: import

Dates and status

Registration Date: Aug 31, 2006
Expiry Date: Aug 31, 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 α1 antitrypsin per reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number accc5fb16541a334b7f929fe36d8989a and manufactured by ORTHO-CLINICAL DIAGNOSTICS, INC.;; ORTHO-CLINICAL DIAGNOSTICS, INC. The authorized representative in Taiwan is DKSH TAIWAN LTD..

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