Taiwan FDA registration a3836ab511adeaf3f1e6eb3c241065ce
Heri Liquid Film (Unsterilized)
TW: 赫麗敷 液體護膜 (未滅菌)
Taiwan·Risk Class 1·AMED CO., LTD.·Registered Jul 08, 2013 – Jul 08, 2028ActiveRegistration details
- Analysis ID
- a3836ab511adeaf3f1e6eb3c241065ce
Company information
- Manufacturer
- AMED CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- AMED CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "Liquid Bandage (J.5090)" Classification and Grading Management Measures for Medical Equipment.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5090 Liquid bandages
- Import Information
- Domestic
Dates and status
- Registration Date
- Jul 08, 2013
- Expiry Date
- Jul 08, 2028
About this record
Access comprehensive regulatory information for Heri Liquid Film (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a3836ab511adeaf3f1e6eb3c241065ce 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.
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