Taiwan FDA registration 1c6cc0a3915ae3b27a27e20a9eaecf6c
"Sudi" Ovulation Rapid Test Reagent (Unsterilized)
TW: “速帝”排卵快速檢驗試劑 (未滅菌)
Taiwan·Risk Class 1·STANDARD DIAGNOSTICS, INC.·Registered Aug 12, 2010 – Aug 12, 2020CancelledRegistration details
- Analysis ID
- 1c6cc0a3915ae3b27a27e20a9eaecf6c
- Customs Code
- DHA04400907902
Company information
- Manufacturer
- STANDARD DIAGNOSTICS, INC.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Abbott Rapid Diagnostics Health Corp.
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
- import
Dates and status
- Registration Date
- Aug 12, 2010
- Expiry Date
- Aug 12, 2020
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Sudi" Ovulation Rapid Test Reagent (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1c6cc0a3915ae3b27a27e20a9eaecf6c and manufactured by STANDARD DIAGNOSTICS, INC.. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health Corp..
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