Taiwan FDA registration f7c5e1b276c508f60d4870180275a72d
Changying human chorionic gonadotropin test reagent
TW: 常盈人類絨毛膜促性腺激素檢驗試劑
Taiwan·Risk Class 2·IMMUNOTECH s.r.o.·Registered Jun 17, 2010 – Jun 17, 2015CancelledRegistration details
- Analysis ID
- f7c5e1b276c508f60d4870180275a72d
- Customs Code
- DHAS0602123104
Company information
- Manufacturer
- IMMUNOTECH s.r.o.
- Manufacturer Country
- Czechia
- Authorized Representative
- WOLCH ENTERPRISES INC.
Product details
- Intended Use
- Quantitative radioimmunoassay was used to determine human pilionic gonadotropin in serum/blood.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1155 Human chorionic gonadotropin testing system
- 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
- Jun 17, 2010
- Expiry Date
- Jun 17, 2015
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Changying human chorionic gonadotropin 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 f7c5e1b276c508f60d4870180275a72d and manufactured by IMMUNOTECH s.r.o.. The authorized representative in Taiwan is WOLCH ENTERPRISES INC..
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