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"I.V. House" UltraDressing (Non-Sterile) - Taiwan Registration 4232d5351df5ea3f4825519d7ef9e4db

Access comprehensive regulatory information for "I.V. House" UltraDressing (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 4232d5351df5ea3f4825519d7ef9e4db and manufactured by I.V. HOUSE, INC.. The authorized representative in Taiwan is MIMED 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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4232d5351df5ea3f4825519d7ef9e4db
Registration Details
Taiwan FDA Registration: 4232d5351df5ea3f4825519d7ef9e4db
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Device Details

"I.V. House" UltraDressing (Non-Sterile)
TW: "ๆ„›ไผ่ญท" ่ก€็ฎกๅ…งๅฐŽ็ฎกๅœ“่“‹ๅ›บๅฎšๅฅ— (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

4232d5351df5ea3f4825519d7ef9e4db

Ministry of Health Medical Device Import No. 016142

DHA09401614203

Company Information

United States

Product Details

Limited to the first level recognition range of endovascular catheter fixation device (J.5210) of the Measures for the Administration of Medical Devices.

J General hospital and personal use equipment

J5210 Endovascular catheter fixation device

Imported from abroad

Dates and Status

Feb 03, 2016

Feb 03, 2021