Taiwan FDA registration 26c4762a0f3fa7c5d6558d77b5501213

"Keris" foam wound dressing (sterilized)

TW: "凱瑞斯" 泡綿傷口敷料 (滅菌)

Taiwan·Risk Class 1·SHI HENG TECHNOLOGY CO., LTD.·Registered Dec 29, 2016 – Dec 29, 2021Cancelled

Registration details

Analysis ID: 26c4762a0f3fa7c5d6558d77b5501213

Company information

Manufacturer: SHI HENG TECHNOLOGY CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: SHI HENG 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: 國產;; QMS/QSD

Dates and status

Registration Date: Dec 29, 2016
Expiry Date: Dec 29, 2021
Cancellation Date: Aug 28, 2023

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Keris" foam wound dressing (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 26c4762a0f3fa7c5d6558d77b5501213 and manufactured by SHI HENG TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is SHI HENG TECHNOLOGY CO., LTD..

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