Taiwan FDA registration c59e65b266d9eec5aa0dd7b167f6d2aa

Sineng Scar Patch (Unsterilized)

TW: 喜能膚疤痕貼片 (未滅菌)

Taiwan·Risk Class 1·Taiwan Dachang Huajia Co., Ltd.;; Ame Life Limited·Registered Mar 16, 2022 – Mar 16, 2027Active

Registration details

Analysis ID: c59e65b266d9eec5aa0dd7b167f6d2aa

Company information

Manufacturer: Taiwan Dachang Huajia Co., Ltd.;; Ame Life Limited
Manufacturer Country: Taiwan, Province of China
Authorized Representative: DKSH TAIWAN LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Classification and Grading of Medical Devices "Scar Treatment Silicone Products (I.4025)".
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;; Domestic

Dates and status

Registration Date: Mar 16, 2022
Expiry Date: Mar 16, 2027

About this record

Access comprehensive regulatory information for Sineng Scar Patch (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c59e65b266d9eec5aa0dd7b167f6d2aa and manufactured by Taiwan Dachang Huajia Co., Ltd.;; Ame Life Limited. The authorized representative in Taiwan is DKSH TAIWAN LTD..

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