Taiwan FDA registration a08af05c4ce567d3d0d685658601e548

"Trinity" Measles virus ELISA Kit (Non-Sterile)

TW: “萃尼諦”麻疹病毒酵素免疫檢驗試劑組 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·TRINITY BIOTECH USA·Registered Feb 06, 2020 – Feb 06, 2025Expired
Registration details
Analysis ID
a08af05c4ce567d3d0d685658601e548
License Form
Ministry of Health Medical Device Import No. 021234
Customs Code
DHA09402123402
Company information
Manufacturer Country
United States
Authorized Representative
TRUGENE DIAGNOSTICS, INC.
Product details
Intended Use
Limited to the first level identification range of the "Measles Virus Serological Reagent (C.3520)" of the Measures for the Administration of Medical Devices.
Product Type (Level 1)
C Immunology and microbiology devices
Product Type (Level 2)
C3520 Measles virus serum reagent
Import Information
Imported from abroad
Dates and status
Registration Date
Feb 06, 2020
Expiry Date
Feb 06, 2025
About this record

Access comprehensive regulatory information for "Trinity" Measles virus ELISA Kit (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a08af05c4ce567d3d0d685658601e548 and manufactured by TRINITY BIOTECH USA. The authorized representative in Taiwan is TRUGENE DIAGNOSTICS, 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