Taiwan FDA registration 3fcbb20109b4d31ed8be00df1fbb9673

"Hercz" scar care silicone sheeting (Non-Sterile)

TW: "凱獅" 疤痕護理矽膠片 (未滅菌)

Taiwan·Risk Class 1·MD·HERCZ REHABILITATION TECHNOLOGY LIMITED·Registered Sep 11, 2019 – Sep 11, 2024Expired

Registration details

Analysis ID: 3fcbb20109b4d31ed8be00df1fbb9673
License Form: Ministry of Health Medical Device Import No. 020851
Customs Code: DHA09402085108

Company information

Manufacturer: HERCZ REHABILITATION TECHNOLOGY LIMITED
Manufacturer Country: Hong Kong
Authorized Representative: Anlida Technology 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: Sep 11, 2019
Expiry Date: Sep 11, 2024

About this record

Access comprehensive regulatory information for "Hercz" scar care silicone sheeting (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 3fcbb20109b4d31ed8be00df1fbb9673 and manufactured by HERCZ REHABILITATION TECHNOLOGY LIMITED. The authorized representative in Taiwan is Anlida Technology Co., Ltd..

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