Taiwan FDA registration b9ce6eb432898bc9e4494abc49b600c3

"Siemens" total immunoglobulin E radioimmunoassay reagent

TW: “西門子”總免疫球蛋白E放射免疫分析試劑

Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered May 13, 2013 – May 13, 2018Cancelled

Registration details

Analysis ID: b9ce6eb432898bc9e4494abc49b600c3
Customs Code: DHAS0602468901

Company information

Manufacturer: SIEMENS HEALTHCARE DIAGNOSTICS INC.
Manufacturer Country: United States
Authorized Representative: SIEMENS LIMITED

Product details

Intended Use: Immunoradiological analysis was used to quantify the total amount of immunoglobulin E in serum.
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: Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)

Dates and status

Registration Date: May 13, 2013
Expiry Date: May 13, 2018
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 "Siemens" total immunoglobulin E radioimmunoassay reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b9ce6eb432898bc9e4494abc49b600c3 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS LIMITED.

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