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Lekang blood glucose testing system - Taiwan Registration f5c18d4d5e9cbf1e861599955eeb01b2

Access comprehensive regulatory information for Lekang blood glucose testing system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f5c18d4d5e9cbf1e861599955eeb01b2 and manufactured by ACON LABORATORIES, INC.. The authorized representative in Taiwan is FOCUS MEDICAL SYSTEM 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.

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f5c18d4d5e9cbf1e861599955eeb01b2
Registration Details
Taiwan FDA Registration: f5c18d4d5e9cbf1e861599955eeb01b2
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Device Details

Lekang blood glucose testing system
TW: ๆจ‚ๅบท่ก€็ณ–ๆธฌ่ฉฆ็ณป็ตฑ
Risk Class 2

Registration Details

f5c18d4d5e9cbf1e861599955eeb01b2

DHA05602554802

Company Information

United States

Product Details

Quantitatively detect the blood glucose value of fingertips, palms and forearm microvascular whole blood, and professional medical personnel can detect the blood glucose value of neonatal microvascular whole blood.

I General, Plastic Surgery & Dermatology;; A Clinical Chemistry and Clinical Toxicology

I.4800 Manual instruments for general surgery; A.1345 Glucose Test System

import

Dates and Status

Nov 19, 2013

Nov 19, 2023