Taiwan FDA registration 38ccd39ef6c162dcc2869a486dbf5614
Ikang Rotavirus (fecal) antigen rapid test reagent
TW: 艾康 輪狀病毒(糞便)抗原快速檢測試劑
Taiwan·Risk Class 1·ACON BIOTECH (HANGZHOU) CO., LTD.·Registered Mar 26, 2010 – Mar 26, 2015CancelledRegistration details
- Analysis ID
- 38ccd39ef6c162dcc2869a486dbf5614
- Customs Code
- DHA04600089602
Company information
- Manufacturer
- ACON BIOTECH (HANGZHOU) CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- Ariel Health Inc
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Polio Virus Serological Reagent (C.3405)".
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3405 Poliomyelitis virus serum reagent
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Mar 26, 2010
- Expiry Date
- Mar 26, 2015
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Ikang Rotavirus (fecal) antigen rapid test reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 38ccd39ef6c162dcc2869a486dbf5614 and manufactured by ACON BIOTECH (HANGZHOU) CO., LTD.. The authorized representative in Taiwan is Ariel Health Inc.
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