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“Mammy Village” Cold Pack (Non-Sterile) - Taiwan Registration 70c9bfe7164edadfcb325dc0d7abc5db

Access comprehensive regulatory information for “Mammy Village” 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 70c9bfe7164edadfcb325dc0d7abc5db and manufactured by MAMMY VILLAGE CO., LTD.. The authorized representative in Taiwan is MAMMY VILLAGE 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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70c9bfe7164edadfcb325dc0d7abc5db
Registration Details
Taiwan FDA Registration: 70c9bfe7164edadfcb325dc0d7abc5db
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Device Details

“Mammy Village” Cold Pack (Non-Sterile)
TW: “六甲村”冷敷袋 (未滅菌)
Risk Class 1
MD

Registration Details

70c9bfe7164edadfcb325dc0d7abc5db

Ministry of Health Medical Device Manufacturing Registration No. 002593

DHY08300259300

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Medical Cold Compress Pack (O.5700)".

o Equipment for physical medicine

O5700 Medical Cold Pack

Produced in Taiwan, China

Dates and Status

Oct 01, 2021

Oct 31, 2024