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"Ulikang" Glass Expo(Not Wiped Out) - Taiwan Registration e36e2b6c769ac551823b6caa892e0fdd

Access comprehensive regulatory information for "Ulikang" Glass Expo(Not Wiped Out) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e36e2b6c769ac551823b6caa892e0fdd and manufactured by BIOFACTOR SP. ZO. O.. The authorized representative in Taiwan is UNIMED PHARMACEUTICAL ENTERPRISE 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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e36e2b6c769ac551823b6caa892e0fdd
Registration Details
Taiwan FDA Registration: e36e2b6c769ac551823b6caa892e0fdd
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Device Details

"Ulikang" Glass Expo(Not Wiped Out)
TW: "ไฝ‘็ซ‹ๅบท" ็Žป้œฒ่‚›้–€่ญท่†œ(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

e36e2b6c769ac551823b6caa892e0fdd

DHA09402337402

Company Information

Poland

Product Details

Limited to the first level identification range of the "Liquid Bandage (J.5090)" Classification and Grading Management Measures for Medical Equipment.

J General hospital and personal use equipment

J.5090 Liquid bandages

Input;; QMS/QSD

Dates and Status

Jan 22, 2024

Jan 22, 2029