Taiwan FDA registration 5ca2ecd6da5c98de879b6a5c3666046b

Innova Demars Scar Gel (Unsterilized)

TW: “英諾威”得瑪絲疤痕凝膠 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·HANSON MEDICAL INC.;; INOVAIL SINGAPORE PTE. LTD.·Registered May 13, 2009 – May 13, 2014Cancelled
Registration details
Analysis ID
5ca2ecd6da5c98de879b6a5c3666046b
Customs Code
DHA04400772701
Company information
Manufacturer Country
United States;;Singapore
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
Contract manufacturing;; input
Dates and status
Registration Date
May 13, 2009
Expiry Date
May 13, 2014
Cancellation Date
Sep 26, 2016
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for Innova Demars Scar Gel (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5ca2ecd6da5c98de879b6a5c3666046b and manufactured by HANSON MEDICAL INC.;; INOVAIL SINGAPORE PTE. LTD.. The authorized representative in Taiwan is Taiwan Branch of Hong Kong Commercial Law Marinke Pharmaceutical 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