Taiwan FDA registration 2d4df7a317ed57f59a5a9f37eadd05aa

"Dening" acne patch (sterilized)

TW: 〝德甯〞痘痘貼(滅菌)

Taiwan·Risk Class 1·Oriental Innovation Development Co., Ltd. Biomedical Factory·Registered Sep 16, 2011 – Sep 16, 2016Cancelled

Registration details

Analysis ID: 2d4df7a317ed57f59a5a9f37eadd05aa

Company information

Manufacturer: Oriental Innovation Development Co., Ltd. Biomedical Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: DURBLIN ENTERPRISE CO., LTD.

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: 委託製造;; QMS/QSD;; 國產

Dates and status

Registration Date: Sep 16, 2011
Expiry Date: Sep 16, 2016
Cancellation Date: Jul 03, 2018

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Dening" 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 2d4df7a317ed57f59a5a9f37eadd05aa and manufactured by Oriental Innovation Development Co., Ltd. Biomedical Factory. The authorized representative in Taiwan is DURBLIN ENTERPRISE CO., LTD..

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