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FLEXI-AID COLD/HOT PACK (Non-Sterile) - Taiwan Registration 076a156a2078d98aa33e0e3164fe793e

Access comprehensive regulatory information for FLEXI-AID COLD/HOT 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 076a156a2078d98aa33e0e3164fe793e and manufactured by TAIWAN STANCH CO., LTD.. The authorized representative in Taiwan is TAIWAN STANCH 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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076a156a2078d98aa33e0e3164fe793e
Registration Details
Taiwan FDA Registration: 076a156a2078d98aa33e0e3164fe793e
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Device Details

FLEXI-AID COLD/HOT PACK (Non-Sterile)
TW: ่ฒๅพท ๅ†ท็†ฑๆ•ทๅขŠ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

076a156a2078d98aa33e0e3164fe793e

Ministry of Health Medical Device Manufacturing No. 007752

Company Information

Taiwan, Province of China

Product Details

o Equipment for physical medicine

O5700 Medical Cold Pack

Produced in Taiwan, China

Dates and Status

May 06, 2019

May 06, 2024

Cancellation Information

Logged out

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