Taiwan FDA registration 33bd42a9e60739e4c980e633bf83033b
“ZUIKO” Hydrocolloid Wound Pad (NON-STERILE)
TW: “日方” 人工皮親水性敷料 (未滅菌)
Taiwan·Risk Class 1·MD·ZUIKO MEDICAL CORPORATION·Registered Oct 29, 2020 – Oct 29, 2025ExpiredRegistration details
- Analysis ID
- 33bd42a9e60739e4c980e633bf83033b
- License Form
- Ministry of Health Medical Device Import No. 022070
- Customs Code
- DHA09402207003
Company information
- Manufacturer
- ZUIKO MEDICAL CORPORATION
- Manufacturer Country
- Japan
- Authorized Representative
- YUAW DER TRADING CO., LTD.
Product details
- Intended Use
- Limited to the first-level identification range of the Measures for the Administration of Medical Devices "Hydrophilic Wound Covering Materials (I.4018)".
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4018 Hydrophilic trauma coverings
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 29, 2020
- Expiry Date
- Oct 29, 2025
About this record
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..
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