Taiwan FDA registration fbeb85df81dc3bf6ccda76f2f73f3a97

"Entec" Aitern self-adhesive silicone sheet (unsterilized)

TW: “恩特科”愛特恩自黏性矽膠片(未滅菌)
Taiwan flagTaiwan·Risk Class 1·M-TECHNOLOGIES·Registered Oct 02, 2009 – Oct 02, 2014Cancelled
Registration details
Analysis ID
fbeb85df81dc3bf6ccda76f2f73f3a97
Customs Code
DHA04400817200
Company information
Manufacturer
M-TECHNOLOGIES
Manufacturer Country
France
Authorized Representative
GLORIA BIOMED CO., LTD.
Product details
Intended Use
Limited to the first level identification range of "Silicone Sheet (I.4025)" of the Measures for the Administration of Medical Devices.
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I.4025 Silicone products for scar treatment
Import Information
import
Dates and status
Registration Date
Oct 02, 2009
Expiry Date
Oct 02, 2014
Cancellation Date
Jun 28, 2018
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "Entec" Aitern self-adhesive silicone sheet (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fbeb85df81dc3bf6ccda76f2f73f3a97 and manufactured by M-TECHNOLOGIES. The authorized representative in Taiwan is GLORIA BIOMED 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