Taiwan FDA registration 54277588c1974736ad4eed033094fa35
“URGO” SANYRENE spray (Non-Sterile)
TW: “薾格” 舒立潤壓瘡預防噴劑 (未滅菌)
Taiwan·Risk Class 1·MD·LABORATOIRES URGO·Registered Aug 04, 2014 – Aug 04, 2024ExpiredRegistration details
- Analysis ID
- 54277588c1974736ad4eed033094fa35
- License Form
- Ministry of Health Medical Device Import No. 014407
- Customs Code
- DHA09401440703
Company information
- Manufacturer
- LABORATOIRES URGO
- Manufacturer Country
- France
- Authorized Representative
- ZUELLIG PHARMA, INC.
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
- Imported from abroad; GMP
Dates and status
- Registration Date
- Aug 04, 2014
- Expiry Date
- Aug 04, 2024
About this record
Access comprehensive regulatory information for “URGO” SANYRENE spray (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 54277588c1974736ad4eed033094fa35 and manufactured by LABORATOIRES URGO. The authorized representative in Taiwan is ZUELLIG PHARMA, INC..
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