Taiwan FDA registration 8858df5ce27f5196ce7df0ce8a4f98b8
In vitro reagent card for the Faler's pregnancy test
TW: 法萊兒驗孕體外試劑卡
Registration details
- Analysis ID
- 8858df5ce27f5196ce7df0ce8a4f98b8
- Customs Code
- DHY00500350909
Company information
- Manufacturer
- Longteng Biotechnology Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- YEA CHANCE ENTERPRISE CO., LTD.
Product details
- Intended Use
- It is used as a test reagent for early diagnosis of pregnancy.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1155 Human chorionic gonadotropin testing system
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Jan 18, 2012
- Expiry Date
- Feb 09, 2016
- Cancellation Date
- May 13, 2016
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for In vitro reagent card for the Faler's pregnancy test in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8858df5ce27f5196ce7df0ce8a4f98b8 and manufactured by Longteng Biotechnology Co., Ltd. The authorized representative in Taiwan is YEA CHANCE ENTERPRISE CO., LTD..
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