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“Liesien” Cushion (Non-Sterile) - Taiwan Registration a6eecea342d2711fee1f314927452801

Access comprehensive regulatory information for “Liesien” 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 a6eecea342d2711fee1f314927452801 and manufactured by SUPRACOR SYSTEMS, INC.. The authorized representative in Taiwan is LIESIEN ENTERPRISE 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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a6eecea342d2711fee1f314927452801
Registration Details
Taiwan FDA Registration: a6eecea342d2711fee1f314927452801
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Device Details

“Liesien” Cushion (Non-Sterile)
TW: “立薪” 氣墊座(未滅菌)
Risk Class 1
MD

Registration Details

a6eecea342d2711fee1f314927452801

Ministry of Health Medical Device Import No. 022632

DHA09402263206

Company Information

United States

Product Details

Limited to the first level identification scope of the "floating cushion (O.3175)" of the Measures for the Classification and Grading Management of Medical Equipment.

o Equipment for physical medicine

O3175 floating seat cushion

Imported from abroad

Dates and Status

Sep 01, 2021

Sep 01, 2026