Taiwan FDA registration 135364e3eabd76e28d30251e176ab6fa
HERADERM Wound Barrier Solution (Non-sterile)
TW: 赫麗敷 傷口保護液 (未滅菌)
Taiwan·Risk Class 1·MD·AMED CO., LTD.·Registered Apr 28, 2021 – Apr 28, 2026ExpiredRegistration details
- Analysis ID
- 135364e3eabd76e28d30251e176ab6fa
- License Form
- Ministry of Health Medical Device Manufacturing No. 009069
Company information
- Manufacturer
- AMED CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- AMED CO., LTD.
Product details
- Intended Use
- Limit the first level identification range of liquid bandages (J.5090) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J5090 Liquid bandages
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Apr 28, 2021
- Expiry Date
- Apr 28, 2026
About this record
Access comprehensive regulatory information for HERADERM Wound Barrier Solution (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 135364e3eabd76e28d30251e176ab6fa and manufactured by AMED CO., LTD.. The authorized representative in Taiwan is AMED 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 DatabasePowered by Pure Global AI89,000+ Devices