Taiwan FDA registration 02ee0edbce27ecacbd921ad968b3e1c7
Disl Cortisol Enzyme Immunoassay Suite
TW: 迪斯爾皮質醇酵素免疫分析套組
Registration details
- Analysis ID
- 02ee0edbce27ecacbd921ad968b3e1c7
- Customs Code
- DHA00601597200
Company information
- Manufacturer
- DIAGNOSTIC SYSTEMS LABORATORIES, INC.
- Manufacturer Country
- United States
- Authorized Representative
- EVERLIGHT BIOTECH(TAIWAN) CO., LTD.
Product details
- Intended Use
- Quantify the amount of endocrinin in the suprarenal gland in serum or blood pump.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1205 Cortisol (hydronephrine, and hydroxycortisol) test system
- Import Information
- import
Dates and status
- Registration Date
- Feb 07, 2006
- Expiry Date
- Feb 07, 2011
- Cancellation Date
- Jan 18, 2013
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Disl Cortisol Enzyme Immunoassay Suite in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 02ee0edbce27ecacbd921ad968b3e1c7 and manufactured by DIAGNOSTIC SYSTEMS LABORATORIES, INC.. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) 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