Taiwan FDA registration 4a2f7d5f8b3dbad987f3bbec47931470

"Venice" gel cold pack (unsterilized)

TW: "威尼斯"凝膠冷敷包(未滅菌)

Taiwan·Risk Class 1·VENICE LABORATORIES CO., LTD.·Registered Oct 01, 2021 – Oct 31, 2025Expired

Registration details

Analysis ID: 4a2f7d5f8b3dbad987f3bbec47931470

Company information

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

Product details

Intended Use: Limited to the classification and grading management of medical equipment, the first level identification range of "Medical Hot and Cold Compress Device (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: Domestic

Dates and status

Registration Date: Oct 01, 2021
Expiry Date: Oct 31, 2025

About this record

Access comprehensive regulatory information for "Venice" gel cold pack (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4a2f7d5f8b3dbad987f3bbec47931470 and manufactured by VENICE LABORATORIES CO., LTD.. The authorized representative in Taiwan is VENICE LABORATORIES CO., LTD..

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