Pure Global

“ZUIKO” Hydrocolloid Wound Pad (NON-STERILE) - Taiwan Registration 33bd42a9e60739e4c980e633bf83033b

Access comprehensive regulatory information for “ZUIKO” Hydrocolloid Wound Pad (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 33bd42a9e60739e4c980e633bf83033b and manufactured by ZUIKO MEDICAL CORPORATION. The authorized representative in Taiwan is YUAW DER TRADING 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
33bd42a9e60739e4c980e633bf83033b
Registration Details
Taiwan FDA Registration: 33bd42a9e60739e4c980e633bf83033b
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“ZUIKO” Hydrocolloid Wound Pad (NON-STERILE)
TW: “日方” 人工皮親水性敷料 (未滅菌)
Risk Class 1
MD

Registration Details

33bd42a9e60739e4c980e633bf83033b

Ministry of Health Medical Device Import No. 022070

DHA09402207003

Company Information

Japan

Product Details

Limited to the first-level identification range of the Measures for the Administration of Medical Devices "Hydrophilic Wound Covering Materials (I.4018)".

I General and plastic surgical devices

I4018 Hydrophilic trauma coverings

Imported from abroad

Dates and Status

Oct 29, 2020

Oct 29, 2025