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"Miraco" Flotation cushion (Non-Sterile) - Taiwan Registration 389660fda20bf6aadca5aa58ae79ff5f

Access comprehensive regulatory information for "Miraco" Flotation cushion (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 389660fda20bf6aadca5aa58ae79ff5f and manufactured by SIFO Healthcare Corporation. The authorized representative in Taiwan is HORIZON INSTRUMENTS 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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389660fda20bf6aadca5aa58ae79ff5f
Registration Details
Taiwan FDA Registration: 389660fda20bf6aadca5aa58ae79ff5f
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Device Details

"Miraco" Flotation cushion (Non-Sterile)
TW: "็พŽๆจ‚ๅ…‹" ๆธ›ๅฃ“ๅๅขŠ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

389660fda20bf6aadca5aa58ae79ff5f

Ministry of Health Medical Device Manufacturing No. 007864

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Floating Cushion (O.3175)".

o Equipment for physical medicine

O3175 floating seat cushion

Produced in Taiwan, China; Contract manufacturing

Dates and Status

Jul 19, 2019

Jul 19, 2024