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Tokyo Koshisha Liquid Plaster (Non-Sterile) - Taiwan Registration b677571b76ed7e4cb3a7289695c2f43c

Access comprehensive regulatory information for Tokyo Koshisha Liquid Plaster (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b677571b76ed7e4cb3a7289695c2f43c and manufactured by TOKYO KOSHISHA CO., LTD.. The authorized representative in Taiwan is KWANG HWA DRUG FACTORY.

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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b677571b76ed7e4cb3a7289695c2f43c
Registration Details
Taiwan FDA Registration: b677571b76ed7e4cb3a7289695c2f43c
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Device Details

Tokyo Koshisha Liquid Plaster (Non-Sterile)
TW: ๆฑไบฌ็”ฒๅญ็คพๆถฒ้ซ”OK็นƒ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

b677571b76ed7e4cb3a7289695c2f43c

Ministry of Health Medical Device Import No. 022316

DHA09402231609

Company Information

Japan

Product Details

Limit the first level identification range of liquid bandages (J.5090) of the Measures for the Administration of Medical Devices.

J General hospital and personal use equipment

J5090 Liquid bandages

Imported from abroad

Dates and Status

Feb 19, 2021

Feb 19, 2026