Taiwan FDA registration d4c92e17c947c15907dad5b7396a3a83

Cimeosil Scar and Laser Gel (Non-Sterile)

TW: 喜美而疤痕凝膠(未滅菌)

Taiwan·Risk Class 1·MD·IMPLANTECH ASSOCIATES INC.·Registered Oct 26, 2018 – Oct 26, 2028Active

Registration details

Analysis ID: d4c92e17c947c15907dad5b7396a3a83
License Form: Ministry of Health Medical Device Import No. 019731
Customs Code: DHA09401973101

Company information

Manufacturer: IMPLANTECH ASSOCIATES INC.
Manufacturer Country: United States
Authorized Representative: MIMED CO., LTD.

Product details

Intended Use: Limited to the first-level recognition range of the Measures for the Administration of Medical Devices "Scar Treatment Silicone Products (I.4025)".
Product Type (Level 1): I General and plastic surgical devices
Product Type (Level 2): I4025 Scar Treatment Silicone Products
Import Information: Imported from abroad

Dates and status

Registration Date: Oct 26, 2018
Expiry Date: Oct 26, 2028

About this record

Access comprehensive regulatory information for Cimeosil Scar and Laser Gel (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 d4c92e17c947c15907dad5b7396a3a83 and manufactured by IMPLANTECH ASSOCIATES INC.. The authorized representative in Taiwan is MIMED 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.