Syncope immunoglobulin fluorescent binder (unsterilized) - Taiwan Registration 88c5b73602684b220574c95a5301a87d
Access comprehensive regulatory information for Syncope immunoglobulin fluorescent binder (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 88c5b73602684b220574c95a5301a87d and manufactured by EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG. The authorized representative in Taiwan is SEEKERS BIOMEDICAL 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.
Device Details
Product Details
Limited to the first level identification scope of "General Purpose Reaction Reagents (B.4010)" under the Measures for the Administration of Medical Devices.
B Hematology, pathology, and genetics
B.4010 Reaction Reagents for General Purposes
import
Dates and Status
May 21, 2010
May 21, 2020
Aug 05, 2022
Cancellation Information
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