Taiwan FDA registration f8f19f9ff43e2cb6bab8ccf1342990a9

Changying dehydroepiandrosterone sulfate test reagent

TW: 常盈脫氫表雄固酮硫酸鹽檢驗試劑
Taiwan flagTaiwan·Risk Class 1·DIAGNOSTIC SYSTEMS LABORATORIES, INC.·Registered May 04, 2006 – May 04, 2011Cancelled
Registration details
Analysis ID
f8f19f9ff43e2cb6bab8ccf1342990a9
Customs Code
DHA04400435702
Company information
Manufacturer Country
United States
Authorized Representative
WOLCH ENTERPRISES INC.
Product details
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1245 Dehydroepiandrosterone (Free and Sulfur Salt) Test System
Import Information
import
Dates and status
Registration Date
May 04, 2006
Expiry Date
May 04, 2011
Cancellation Date
Nov 26, 2012
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for Changying dehydroepiandrosterone sulfate test reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f8f19f9ff43e2cb6bab8ccf1342990a9 and manufactured by DIAGNOSTIC SYSTEMS LABORATORIES, INC.. 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