Taiwan FDA registration d2e7b2a2fca2eef91bb32f739bf120fe

Mentholedon Acne Patch (Sterilized)

TW: 曼秀雷敦痘痘貼(滅菌)
Taiwan flagTaiwan·Risk Class 1·BenQ Materials Co., Ltd. Taoyuan Plant;; Taiwan Mentholatum Co., Ltd·Registered Aug 12, 2022 – Aug 12, 2027Active
Registration details
Analysis ID
d2e7b2a2fca2eef91bb32f739bf120fe
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
MENTHOLATUM TAIWAN LIMITED
Product details
Intended Use
Limited to the first level recognition range of the classification and grading management measures for medical equipment "hydrophilic trauma 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
委託製造;; QMS/QSD;; 國產
Dates and status
Registration Date
Aug 12, 2022
Expiry Date
Aug 12, 2027
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About this record

Access comprehensive regulatory information for Mentholedon 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 d2e7b2a2fca2eef91bb32f739bf120fe and manufactured by BenQ Materials Co., Ltd. Taoyuan Plant;; Taiwan Mentholatum Co., Ltd. The authorized representative in Taiwan is MENTHOLATUM TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BenQ Materials Co., Ltd. Taoyuan Plant;; Taiwan Mentholatum Co., Ltd, and 1 recent registrations in the same category. 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.

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