Taiwan FDA registration 2dd29036cf952c583c44a415847c5cd5
Unified DIY automatic detection series
TW: 統一DIY自動檢測系列
Taiwan·Risk Class 2·Lianshang Biotechnology Co., Ltd. Wugu Factory·Registered May 16, 2006 – May 16, 2011CancelledRegistration details
- Analysis ID
- 2dd29036cf952c583c44a415847c5cd5
- Customs Code
- DHY00500205402
Company information
- Manufacturer
- Lianshang Biotechnology Co., Ltd. Wugu Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PRESIDENT PHARMACEUTICAL CORPORATION
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
- May 16, 2006
- Expiry Date
- May 16, 2011
- Cancellation Date
- Nov 01, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Unified DIY automatic detection series in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2dd29036cf952c583c44a415847c5cd5 and manufactured by Lianshang Biotechnology Co., Ltd. Wugu Factory. The authorized representative in Taiwan is PRESIDENT PHARMACEUTICAL CORPORATION.
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