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"I.V. House" TLC UltraSplint (Non-Sterile) - Taiwan Registration ceeb3faf37f9347d63286b75bf79156a

Access comprehensive regulatory information for "I.V. House" TLC UltraSplint (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 ceeb3faf37f9347d63286b75bf79156a 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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ceeb3faf37f9347d63286b75bf79156a
Registration Details
Taiwan FDA Registration: ceeb3faf37f9347d63286b75bf79156a
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Device Details

"I.V. House" TLC UltraSplint (Non-Sterile)
TW: "ๆ„›ไผ่ญท" ๅ›บๅฎšๆฟ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

ceeb3faf37f9347d63286b75bf79156a

Ministry of Health Medical Device Import No. 016153

DHA09401615308

Company Information

United States

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Splints for Non-Expanded Limbs (I.3910)".

I General and plastic surgical devices

I3910 Splints for non-inflated extremities

Imported from abroad

Dates and Status

Feb 05, 2016

Feb 05, 2021