Taiwan FDA registration 7dd2163ad747403da99f590a26e5ba94
Whole Valley Precision Pregnancy Test Reagent
TW: 全谷精準驗孕試劑
Taiwan·Risk Class 2·Lianshang Biotechnology Co., Ltd. Wugu Factory·Registered Aug 10, 2006 – Aug 10, 2011CancelledRegistration details
- Analysis ID
- 7dd2163ad747403da99f590a26e5ba94
- Customs Code
- DHY00500216804
Company information
- Manufacturer
- Lianshang Biotechnology Co., Ltd. Wugu Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Whole Valley Biotechnology Co., Ltd
Product details
- Intended Use
- Rapid immunoassay was used to detect human placental chorionic gonadal hormone in urine.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1155 Human chorionic gonadotropin testing system
- Import Information
- Domestic
Dates and status
- Registration Date
- Aug 10, 2006
- Expiry Date
- Aug 10, 2011
- Cancellation Date
- Oct 25, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Whole Valley Precision Pregnancy 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 7dd2163ad747403da99f590a26e5ba94 and manufactured by Lianshang Biotechnology Co., Ltd. Wugu Factory. The authorized representative in Taiwan is Whole Valley Biotechnology Co., Ltd.
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