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"I.V. House" UltraDome (Non-Sterile) - Taiwan Registration 2bb5e7de4bffef227077fa2d7cce8400

Access comprehensive regulatory information for "I.V. House" UltraDome (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 2bb5e7de4bffef227077fa2d7cce8400 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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2bb5e7de4bffef227077fa2d7cce8400
Registration Details
Taiwan FDA Registration: 2bb5e7de4bffef227077fa2d7cce8400
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Device Details

"I.V. House" UltraDome (Non-Sterile)
TW: "ๆ„›ไผ่ญท" ่ก€็ฎกๅ…งๅฐŽ็ฎก้˜ฒ่ญทๅฅ— (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

2bb5e7de4bffef227077fa2d7cce8400

Ministry of Health Medical Device Import No. 016141

DHA09401614101

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