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"Venice" Gel Cold Pack (Non-sterile) - Taiwan Registration 9261000f1c3505822e644d0c5bbd5c00

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..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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9261000f1c3505822e644d0c5bbd5c00
Registration Details
Taiwan FDA Registration: 9261000f1c3505822e644d0c5bbd5c00
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Device Details

"Venice" Gel Cold Pack (Non-sterile)
TW: "ๅจๅฐผๆ–ฏ"ๅ‡่† ๅ†ทๆ•ทๅŒ…(ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

9261000f1c3505822e644d0c5bbd5c00

Ministry of Health Medical Device Manufacturing No. 007033

Company Information

Taiwan, Province of China

Product Details

o Equipment for physical medicine

O5700 Medical Cold Pack

Produced in Taiwan, China

Dates and Status

Nov 27, 2017

Nov 27, 2022

Cancellation Information

Logged out

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