Pure Global

GB Troponin I EIA Kit - Taiwan Registration 4dd73e529903d1e70472d3684e6c2e3b

Access comprehensive regulatory information for GB Troponin I EIA Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4dd73e529903d1e70472d3684e6c2e3b and manufactured by BIOCHECK, INC.. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..

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 Database
Powered by Pure Global AI
89,000+ Devices
4dd73e529903d1e70472d3684e6c2e3b
Registration Details
Taiwan FDA Registration: 4dd73e529903d1e70472d3684e6c2e3b
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

GB Troponin I EIA Kit
TW: ๆ™ฎ็”Ÿ่‚Œ้ˆฃ่›‹็™ฝI้…ต็ด ๅ…็–ซๅˆ†ๆžๅฅ—็ต„
Risk Class 2
MD

Registration Details

4dd73e529903d1e70472d3684e6c2e3b

Ministry of Health Medical Device Import No. 027692

DHA05602769203

Company Information

United States

Product Details

Quantitatively determine the concentration of human serum central troponin I (cTnI).

A Clinical chemistry and clinical toxicology

A1215 Creatine phosphocatalyzed?/creatine excitation or isomeric test system

Imported from abroad

Dates and Status

Sep 24, 2015

Sep 24, 2025