Taiwan FDA registration e8a03684ee257e203545e8d2fa48b3ec

"Azusa Source" hydrophilic wound litter (sterilization)

TW: “梓源”親水性傷口敷料 (滅菌)

Taiwan·Risk Class 1·Oriental Innovation Development Co., Ltd. Biomedical Factory·Registered Jul 04, 2012 – Jul 04, 2017Cancelled

Registration details

Analysis ID: e8a03684ee257e203545e8d2fa48b3ec

Company information

Manufacturer: Oriental Innovation Development Co., Ltd. Biomedical Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Human Origin Biotechnology 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;; 國產;; QMS/QSD

Dates and status

Registration Date: Jul 04, 2012
Expiry Date: Jul 04, 2017
Cancellation Date: Nov 15, 2019

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Azusa Source" hydrophilic wound litter (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e8a03684ee257e203545e8d2fa48b3ec and manufactured by Oriental Innovation Development Co., Ltd. Biomedical Factory. The authorized representative in Taiwan is Human Origin Biotechnology Co.,Ltd.

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