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"Arkra" aspartate transamine test strip per test - Taiwan Registration 18a51cd5289b5090e9047c7105ebb7e9

Access comprehensive regulatory information for "Arkra" aspartate transamine test strip per test in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 18a51cd5289b5090e9047c7105ebb7e9 and manufactured by ARKRAY Factory, Inc., Head office factory. The authorized representative in Taiwan is SYNGEN BIOTECH 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.

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18a51cd5289b5090e9047c7105ebb7e9
Registration Details
Taiwan FDA Registration: 18a51cd5289b5090e9047c7105ebb7e9
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Device Details

"Arkra" aspartate transamine test strip per test
TW: "ๆ„›็ง‘ไพ†"ๅคฉ้–€ๅ†ฌ่ƒบ้…ธ่ฝ‰่ƒบๆฏๆชขๆธฌ่ฉฆ็ด™
Risk Class 2

Registration Details

18a51cd5289b5090e9047c7105ebb7e9

DHA00601569806

Company Information

Product Details

SPOTCHEM II GT trial is a test-tube diagnostic test drug that uses serum or plasma for quantitative determination of GET. This product is dedicated to SPOTCHEM instruments.

A Clinical chemistry and clinical toxicology

A.1100 ๅคฉ้–€ๅ†ฌ่ƒบ้…ธ่ฝ‰่ƒบ้…ถ่ฉฆ้ฉ—็ณป็ตฑ

import

Dates and Status

Dec 20, 2005

Dec 20, 2025