Taiwan FDA registration ec8ce05cdefb866d228f1c5a2b8543bc

Anthoreten Acne Patch (Sterilized)

TW: 曼秀雷敦痘痘貼 (滅菌)

Taiwan·Risk Class 1·Oriental Innovation Development Co., Ltd. Biomedical Factory·Registered Mar 06, 2013 – Mar 06, 2023Expired

Registration details

Analysis ID: ec8ce05cdefb866d228f1c5a2b8543bc

Company information

Manufacturer: Oriental Innovation Development Co., Ltd. Biomedical Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: MENTHOLATUM TAIWAN LIMITED

Product details

Intended Use: Limited to the first-level identification range of the Measures for the Administration of Medical Devices "Hydrophilic Wound Covering Materials (I.4018)".
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4018 親水性創傷覆蓋材
Import Information: 國產;; 委託製造;; QMS/QSD

Dates and status

Registration Date: Mar 06, 2013
Expiry Date: Mar 06, 2023

About this record

Access comprehensive regulatory information for Anthoreten Acne Patch (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ec8ce05cdefb866d228f1c5a2b8543bc and manufactured by Oriental Innovation Development Co., Ltd. Biomedical Factory. The authorized representative in Taiwan is MENTHOLATUM TAIWAN LIMITED.

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.