Taiwan FDA registration 1692ec5eaa80824ff82173f1e423adf2
Daian Shaoyun luteinizing hormone analysis reagent
TW: 岱安韶韻黃體生成激素分析試劑
Registration details
- Analysis ID
- 1692ec5eaa80824ff82173f1e423adf2
- Customs Code
- DHAS0601659802
Company information
- Manufacturer
- DIASORIN S.P.A.
- Manufacturer Country
- Italy
- Authorized Representative
- NEW SCIENTIFIC EQUIPMENT CO., LTD.
Product details
- Intended Use
- In vitro measurement of the amount of immune radiation to luteinizing hormone in human serum and plasma.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1485 Progesterone testing system
- Import Information
- Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)
Dates and status
- Registration Date
- May 18, 2006
- Expiry Date
- May 18, 2011
- Cancellation Date
- Oct 26, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Daian Shaoyun luteinizing hormone analysis reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1692ec5eaa80824ff82173f1e423adf2 and manufactured by DIASORIN S.P.A.. The authorized representative in Taiwan is NEW SCIENTIFIC EQUIPMENT CO., LTD..
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