Taiwan FDA registration 41a5b91ef14910b189a64d0f25f12392

Esther Debridement Gel (Sterilized)

TW: 〝以斯帖〞清創修護凝膠(滅菌)

Taiwan·Risk Class 1·Oriental Innovation Development Co., Ltd. Biomedical Factory·Registered Apr 20, 2012 – Apr 20, 2017Cancelled

Registration details

Analysis ID: 41a5b91ef14910b189a64d0f25f12392

Company information

Manufacturer: Oriental Innovation Development Co., Ltd. Biomedical Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: ESTHER MATERIAL TECHNOLOGY 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: QMS/QSD;; 國產;; 委託製造

Dates and status

Registration Date: Apr 20, 2012
Expiry Date: Apr 20, 2017
Cancellation Date: Dec 13, 2019

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for Esther Debridement Gel (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 41a5b91ef14910b189a64d0f25f12392 and manufactured by Oriental Innovation Development Co., Ltd. Biomedical Factory. The authorized representative in Taiwan is ESTHER MATERIAL TECHNOLOGY CO., LTD..

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