Taiwan FDA registration ff0f25e971645d54af283a4f631e8a66
"Everying" Follicle Stimulating Hormone Detection Reagent (Unsterilized)
TW: "常盈" 卵泡刺激激素檢測試劑 (未滅菌)
Registration details
- Analysis ID
- ff0f25e971645d54af283a4f631e8a66
- Customs Code
- DHA04401276500
Company information
- Manufacturer
- IMMUNOTECH s.r.o.
- Manufacturer Country
- Czechia
- Authorized Representative
- WOLCH ENTERPRISES INC.
Product details
- Intended Use
- Limited to the first level of identification scope of the "Follicle stimulating test system (A.1300)" of the medical device management method.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1300 Follicular Stimulation Hormone Test System
- Import Information
- import
Dates and status
- Registration Date
- Mar 04, 2013
- Expiry Date
- Mar 04, 2018
- Cancellation Date
- Nov 17, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Everying" Follicle Stimulating Hormone Detection 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 ff0f25e971645d54af283a4f631e8a66 and manufactured by IMMUNOTECH s.r.o.. The authorized representative in Taiwan is WOLCH ENTERPRISES INC..
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