Taiwan FDA registration 6b5de124d34dbfb307624ace64fe1561
"Everydory" ovulation in vitro reagent set (unsterilized)
TW: “益多利” 排卵體外試劑組 (未滅菌)
Taiwan·Risk Class 1·Longteng Biotechnology Co., Ltd. new market factory·Registered Apr 13, 2018 – Apr 13, 2023CancelledRegistration details
- Analysis ID
- 6b5de124d34dbfb307624ace64fe1561
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Estori Corporation Limited
Product details
- Intended Use
- Limited to the first level recognition range of the "Luteinizing hormone test system (A.1485)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1485 Progesterone testing system
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Apr 13, 2018
- Expiry Date
- Apr 13, 2023
- Cancellation Date
- May 18, 2020
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Everydory" ovulation in vitro reagent set (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6b5de124d34dbfb307624ace64fe1561 and manufactured by Longteng Biotechnology Co., Ltd. new market factory. The authorized representative in Taiwan is Estori Corporation Limited.
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