Taiwan FDA registration 7ba95b5de4b33773fbb11c9b2b352d57

"Siemens" complement test reagent

TW: “西門子” 補體檢驗試劑

Taiwan·Risk Class 2·RANDOX LABORATORIES LTD.;; Siemens Healthcare Diagnostics Inc.·Registered Nov 19, 2018 – Nov 19, 2028Active

Registration details

Analysis ID: 7ba95b5de4b33773fbb11c9b2b352d57
Customs Code: DHA05603179502

Company information

Manufacturer: RANDOX LABORATORIES LTD.;; Siemens Healthcare Diagnostics Inc.
Manufacturer Country: United Kingdom;;United States
Authorized Representative: SIEMENS HEALTHCARE LIMITED

Product details

Intended Use: This product is used in vitro diagnostics and needs to be used with Atellica CH Analyzer to quantitatively detect complement C3 in human serum.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.5240 補體成份免疫試驗系統
Import Information: import

Dates and status

Registration Date: Nov 19, 2018
Expiry Date: Nov 19, 2028

About this record

Access comprehensive regulatory information for "Siemens" complement test reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7ba95b5de4b33773fbb11c9b2b352d57 and manufactured by RANDOX LABORATORIES LTD.;; Siemens Healthcare Diagnostics Inc.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

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