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"Bioken" Dense LDL Cholesterol Test Reagent (Unsterilized) - Taiwan Registration f6c92f91abaa4af1cfbf122e1f9c3cae

Access comprehensive regulatory information for "Bioken" Dense LDL Cholesterol Test 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 f6c92f91abaa4af1cfbf122e1f9c3cae and manufactured by DENKA CO., LTD. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.

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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f6c92f91abaa4af1cfbf122e1f9c3cae
Registration Details
Taiwan FDA Registration: f6c92f91abaa4af1cfbf122e1f9c3cae
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Device Details

"Bioken" Dense LDL Cholesterol Test Reagent (Unsterilized)
TW: ใ€็”Ÿ็ ”ใ€ž็ทปๅฏ†ไฝŽๅฏ†ๅบฆ่„‚่›‹็™ฝ่†ฝๅ›บ้†‡ๆชข้ฉ—่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

f6c92f91abaa4af1cfbf122e1f9c3cae

DHA04401115303

Company Information

Japan

Product Details

Limited to the classification and grading management method of medical equipment, lipoprotein test system (A.1475) first level recognition range.

A Clinical chemistry and clinical toxicology

A.1475 Lipoprotein Testing System

import

Dates and Status

Dec 07, 2011

Dec 07, 2026