Taiwan FDA registration ce2af82dffcd4a563e88af5f6c1e06fd
"Ear fruit suction" non-adhesive lipoglial wound dressing (sterilized)
TW: “耳果悠立吸”非黏著式脂膠質創傷敷料 (滅菌)
Taiwan·Risk Class 1·URGO LABORATORIES·Registered Jul 19, 2006 – Jul 19, 2011CancelledRegistration details
- Analysis ID
- ce2af82dffcd4a563e88af5f6c1e06fd
- Customs Code
- DHA04400492908
Company information
- Manufacturer
- URGO LABORATORIES
- Manufacturer Country
- France
- Authorized Representative
- Ariel Health Inc
Product details
- Intended Use
- It is limited to the first level of identification scope of the medical device management measures "Hydrophilic Wound Covering Materials (I.4018)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4018 親水性創傷覆蓋材
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Jul 19, 2006
- Expiry Date
- Jul 19, 2011
- Cancellation Date
- Nov 06, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Ear fruit suction" non-adhesive lipoglial wound dressing (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ce2af82dffcd4a563e88af5f6c1e06fd and manufactured by URGO LABORATORIES. The authorized representative in Taiwan is Ariel Health 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