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"Essens" rapid blood glucose test unit II - Taiwan Registration 1c7ad21df98e2b6a5280ddf8f7ca6ec0

Access comprehensive regulatory information for "Essens" rapid blood glucose test unit II in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1c7ad21df98e2b6a5280ddf8f7ca6ec0 and manufactured by i-SENS, Wonju Factory. The authorized representative in Taiwan is I CHIANG INSTRUMENT CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including I โ€“ SENS, INC., and 1 recent registrations in the same category. 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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1c7ad21df98e2b6a5280ddf8f7ca6ec0
Registration Details
Taiwan FDA Registration: 1c7ad21df98e2b6a5280ddf8f7ca6ec0
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Device Details

"Essens" rapid blood glucose test unit II
TW: "ๆ„›ๆฃฎๆ–ฏ"ๅฟซ้€Ÿๆธฌ่ก€็ณ–ๆฉŸ็ต„II
Risk Class 2
Cancelled

Registration Details

1c7ad21df98e2b6a5280ddf8f7ca6ec0

DHA00602167404

Company Information

Korea, Republic of

Product Details

Measure the concentration of glucose in the blood.

A Clinical chemistry and clinical toxicology

A.1345 Glucose Test System

Dates and Status

Nov 02, 2010

Nov 02, 2020

Jun 17, 2023

Cancellation Information

Logged out

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