Taiwan FDA registration 1987c32aaa265042acd26587694096e3

"Siemens" protein corrector

TW: "西門子" 蛋白質校正品

Taiwan·Risk Class 2·Siemens Healthcare Diagnostics Products GmbH;; Siemens Healthcare Diagnostics Inc.·Registered Jul 11, 2024 – Jul 11, 2029Active

Registration details

Analysis ID: 1987c32aaa265042acd26587694096e3
Customs Code: DHA05603708807

Company information

Manufacturer: Siemens Healthcare Diagnostics Products GmbH;; Siemens Healthcare Diagnostics Inc.
Manufacturer Country: United States;;Germany
Authorized Representative: SIEMENS HEALTHCARE LIMITED

Product details

Intended Use: 本產品用於體外診斷用途,搭配 Atellica 化學分析儀來校正 Atellica CH Anti-Streptolysin-O_3 (ASO_3)試驗.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1150 Calibrated Products
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: Jul 11, 2024
Expiry Date: Jul 11, 2029

About this record

Access comprehensive regulatory information for "Siemens" protein corrector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1987c32aaa265042acd26587694096e3 and manufactured by Siemens Healthcare Diagnostics Products GmbH;; Siemens Healthcare Diagnostics Inc.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

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