Taiwan FDA registration 1d4b733e732a672ebe41cd5c7bf9e65f
"Amity" Ovulation Test Reagent (Unsterilized)
TW: "愛德" 排卵檢測試劑 (未滅菌)
Registration details
- Analysis ID
- 1d4b733e732a672ebe41cd5c7bf9e65f
- Customs Code
- DHA09600281709
Company information
- Manufacturer
- AIDE DIAGNOSTIC CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- WEIYOU TECH INC.
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
- Input;; Chinese goods
Dates and status
- Registration Date
- Aug 11, 2016
- Expiry Date
- Aug 11, 2021
- Cancellation Date
- Oct 06, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Amity" Ovulation 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 1d4b733e732a672ebe41cd5c7bf9e65f and manufactured by AIDE DIAGNOSTIC CO., LTD.. The authorized representative in Taiwan is WEIYOU TECH INC..
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