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Medifoam Pro N - Taiwan Registration 102f42dfb8ba608b2a14ffa80dee5494

Access comprehensive regulatory information for Medifoam Pro N in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 102f42dfb8ba608b2a14ffa80dee5494 and manufactured by Genewel Co., Ltd.. The authorized representative in Taiwan is CHI FU TRADING 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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102f42dfb8ba608b2a14ffa80dee5494
Registration Details
Taiwan FDA Registration: 102f42dfb8ba608b2a14ffa80dee5494
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Device Details

Medifoam Pro N
TW: ็พŽ่ฟช่Šณ็ข˜ๆณกๆฃ‰ๆ•ทๆ–™
Risk Class 2
MD

Registration Details

102f42dfb8ba608b2a14ffa80dee5494

Ministry of Health Medical Device Import No. 032672

DHA05603267204

Company Information

Korea, Republic of

Product Details

For details, it is Chinese approved copy of the imitation order

I General and plastic surgical devices

I4020 Wound/burn dressings for closure

Imported from abroad

Dates and Status

May 23, 2019

May 23, 2024