Taiwan FDA registration fe1e5de7054a8875526bc3175a25b6f2
"Shengyue" ovulation in vitro reagent card (unsterilized)
TW: “盛悅”排卵體外試劑卡 (未滅菌)
Taiwan·Risk Class 1·The first factory of Longteng Biotechnology Co., Ltd·Registered Feb 14, 2014 – Feb 14, 2019CancelledRegistration details
- Analysis ID
- fe1e5de7054a8875526bc3175a25b6f2
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PHARMAZON CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "luteinizing hormone test system (A.1485)" of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1485 Progesterone testing system
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Feb 14, 2014
- Expiry Date
- Feb 14, 2019
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Shengyue" ovulation in vitro reagent card (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fe1e5de7054a8875526bc3175a25b6f2 and manufactured by The first factory of Longteng Biotechnology Co., Ltd. The authorized representative in Taiwan is PHARMAZON CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices