Taiwan FDA registration 20b6b17a0ebcae0b5273af7b85f65d53

"Hengyang" cold compress (unsterilized)

TW: "恆陽" 冷敷貼 (未滅菌)

Taiwan·Risk Class 1·VENICE LABORATORIES CO., LTD.·Registered Aug 23, 2016 – Aug 23, 2021Cancelled

Registration details

Analysis ID: 20b6b17a0ebcae0b5273af7b85f65d53

Company information

Manufacturer: VENICE LABORATORIES CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: SOLARIS BIOPHARMA CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Medical Cold Compress Pack (O.5700)".
Product Type (Level 1): o Physical Medical Sciences
Product Type (Level 2): O.5700 醫療用冷熱敷裝置
Import Information: Contract manufacturing;; Domestic

Dates and status

Registration Date: Aug 23, 2016
Expiry Date: Aug 23, 2021
Cancellation Date: Sep 19, 2023

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for "Hengyang" cold compress (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 20b6b17a0ebcae0b5273af7b85f65d53 and manufactured by VENICE LABORATORIES CO., LTD.. The authorized representative in Taiwan is SOLARIS BIOPHARMA CO., LTD..

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