Taiwan FDA registration 83d2814f98a513dc929237a682bca586
"Evergreen" progesterone detection reagent (unsterilized)
TW: "常盈" 黃體激素檢測試劑 (未滅菌)
Taiwan·Risk Class 1·IMMUNOTECH s.r.o.·Registered Mar 04, 2013 – Mar 04, 2018CancelledRegistration details
- Analysis ID
- 83d2814f98a513dc929237a682bca586
- Customs Code
- DHA04401276401
Company information
- Manufacturer
- IMMUNOTECH s.r.o.
- Manufacturer Country
- Czechia
- Authorized Representative
- WOLCH ENTERPRISES 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
- 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 "Evergreen" progesterone 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 83d2814f98a513dc929237a682bca586 and manufactured by IMMUNOTECH s.r.o.. The authorized representative in Taiwan is WOLCH ENTERPRISES 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