Taiwan FDA registration 9261000f1c3505822e644d0c5bbd5c00

"Venice" Gel Cold Pack (Non-sterile)

TW: "威尼斯"凝膠冷敷包(未滅菌)

Taiwan·Risk Class 1·MD·VENICE LABORATORIES CO., LTD.·Registered Nov 27, 2017 – Nov 27, 2022Cancelled

Registration details

Analysis ID: 9261000f1c3505822e644d0c5bbd5c00
License Form: Ministry of Health Medical Device Manufacturing No. 007033

Company information

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

Product details

Product Type (Level 1): o Equipment for physical medicine
Product Type (Level 2): O5700 Medical Cold Pack
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Nov 27, 2017
Expiry Date: Nov 27, 2022

Cancellation information

Status: Logged out
Reason: 轉為登錄字號

About this record

Access comprehensive regulatory information for "Venice" Gel Cold Pack (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9261000f1c3505822e644d0c5bbd5c00 and manufactured by VENICE LABORATORIES CO., LTD.. The authorized representative in Taiwan is VENICE LABORATORIES CO., LTD..

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