Taiwan FDA registration ea5350d40ae5600fb25c1924bd27bcae

Ikang tuberculosis antibody (whole blood/serum/plasma) detection reagent

TW: 艾康結核抗體(全血/血清/血漿)檢測試劑

Taiwan·Risk Class 1·ACON BIOTECH (HANGZHOU) CO., LTD.·Registered Sep 19, 2006 – Sep 19, 2011Cancelled

Registration details

Analysis ID: ea5350d40ae5600fb25c1924bd27bcae
Customs Code: DHA04600029502

Company information

Manufacturer: ACON BIOTECH (HANGZHOU) CO., LTD.
Manufacturer Country: China
Authorized Representative: GENERAL BIOLOGICALS CORP.

Product details

Intended Use: Chromatography immunochromatography is used as an adjunct to the testing of specific antibodies to Mycobacterium tuberculosis flora in human whole blood, serum, and plasma. The results of this test should be determined in conjunction with the report of other test methods and the clinical symptoms of the subject.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3370 結核桿菌免疫螢光試劑
Import Information: Chinese goods;; input

Dates and status

Registration Date: Sep 19, 2006
Expiry Date: Sep 19, 2011
Cancellation Date: Nov 28, 2012

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for Ikang tuberculosis antibody (whole blood/serum/plasma) detection reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ea5350d40ae5600fb25c1924bd27bcae and manufactured by ACON BIOTECH (HANGZHOU) CO., LTD.. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..

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