Taiwan FDA registration 08f08f38113703d053a7022552154e92

"Doctor Derma" silicone gel (Non-sterile)

TW: "韓得美" 疤痕護理凝膠 (未滅菌)

Taiwan·Risk Class 1·MD·SUNGJI MEDICAL CO.·Registered Jan 19, 2017 – Jan 19, 2027Active

Registration details

Analysis ID: 08f08f38113703d053a7022552154e92
License Form: Ministry of Health Medical Device Import No. 017441
Customs Code: DHA09401744105

Company information

Manufacturer: SUNGJI MEDICAL CO.
Manufacturer Country: Korea, Republic of
Authorized Representative: HORIZON INSTRUMENTS 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: Jan 19, 2017
Expiry Date: Jan 19, 2027

About this record

Access comprehensive regulatory information for "Doctor Derma" silicone 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 08f08f38113703d053a7022552154e92 and manufactured by SUNGJI MEDICAL CO.. The authorized representative in Taiwan is HORIZON INSTRUMENTS 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.