Taiwan FDA registration 54d8a7a2752ca49df0f3802de6e68059
Keris Polyvinyl Foam Wound Dressing (Sterilized)
TW: 凱瑞斯 聚乙烯醇泡綿傷口敷料 (滅菌)
Taiwan·Risk Class 1·SHI HENG TECHNOLOGY CO., LTD.·Registered Jun 04, 2016 – Jun 04, 2021CancelledRegistration details
- Analysis ID
- 54d8a7a2752ca49df0f3802de6e68059
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
- Jun 04, 2016
- Expiry Date
- Jun 04, 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 Polyvinyl 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 54d8a7a2752ca49df0f3802de6e68059 and manufactured by SHI HENG TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is SHI HENG TECHNOLOGY CO., LTD..
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