Taiwan FDA registration 2b8a556264151ebb55447e65b85bb8fd

"Siemens" total immunoglobulin E quality control solution

TW: “西門子”總量免疫球蛋白E品管液

Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED·Registered Oct 28, 2008 – Oct 28, 2018Cancelled

Registration details

Analysis ID: 2b8a556264151ebb55447e65b85bb8fd
Customs Code: DHA00601947302

Company information

Manufacturer: SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED
Manufacturer Country: United Kingdom
Authorized Representative: SIEMENS LIMITED

Product details

Intended Use: 此品管液為已分析的雙濃度總量免疫球蛋白E品管液,專用於Coat-A-Count IRMA、IMMULITE / IMMULITE 1000、IMMULITE 2000 和 IMMULITE 2500 的Total IgE 檢測法,可用來輔助監視每日的分析表現.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.5510 免疫球蛋白A,G,M,D及E免疫試驗系統
Import Information: import

Dates and status

Registration Date: Oct 28, 2008
Expiry Date: Oct 28, 2018
Cancellation Date: Apr 10, 2020

Cancellation information

Status: Logged out
Reason: 公司歇業

About this record

Access comprehensive regulatory information for "Siemens" total immunoglobulin E quality control solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2b8a556264151ebb55447e65b85bb8fd and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED. The authorized representative in Taiwan is SIEMENS LIMITED.

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