Taiwan FDA registration f4d163fb8bcbac3a593a29f72ce07686

"Mestark" General Purpose Reaction Reagent (Unsterilized)

TW: “麥斯塔克”一般目的反應試劑(未滅菌)
Taiwan flagTaiwan·Risk Class 1·AMERICAN MASTERTECH SCIENTIFIC, INC.·Registered Jun 06, 2012 – Jun 06, 2017Cancelled
Registration details
Analysis ID
f4d163fb8bcbac3a593a29f72ce07686
Customs Code
DHA04401179800
Company information
Manufacturer Country
United States
Authorized Representative
Youtaiji Biotechnology Co., Ltd
Product details
Intended Use
Limited to the first level identification scope of "General Purpose Reaction Reagents (B.4010)" under the Measures for the Administration of Medical Devices.
Product Type (Level 1)
B Hematology, pathology, and genetics
Product Type (Level 2)
B.4010 Reaction Reagents for General Purposes
Import Information
import
Dates and status
Registration Date
Jun 06, 2012
Expiry Date
Jun 06, 2017
Cancellation Date
Jun 03, 2017
Cancellation information
Status
Logged out
Reason
公司歇業
About this record

Access comprehensive regulatory information for "Mestark" General Purpose Reaction 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 f4d163fb8bcbac3a593a29f72ce07686 and manufactured by AMERICAN MASTERTECH SCIENTIFIC, INC.. The authorized representative in Taiwan is Youtaiji Biotechnology 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