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"KEISEI" Powered flotation therapy bed (Non-Sterile) - Taiwan Registration b562f957a74a61532eec1948dc3aba03

Access comprehensive regulatory information for "KEISEI" Powered flotation therapy bed (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 b562f957a74a61532eec1948dc3aba03 and manufactured by KEISEI MEDICAL INDUSTRIAL CO., LTD. The authorized representative in Taiwan is CHIUYU MEDICAL CO., LTD..

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b562f957a74a61532eec1948dc3aba03
Registration Details
Taiwan FDA Registration: b562f957a74a61532eec1948dc3aba03
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Device Details

"KEISEI" Powered flotation therapy bed (Non-Sterile)
TW: "ไบฌๆˆ" ๅ‹•ๅŠ›ๅผๆฐฃๆตๆผ‚ๆตฎๆฒป็™‚ๅบŠ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

b562f957a74a61532eec1948dc3aba03

Ministry of Health Medical Device Import No. 017055

DHA09401705500

Company Information

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Powered Airflow Floating Treatment Bed (O.5170)".

o Equipment for physical medicine

O5170 powered airflow floating treatment bed

Imported from abroad

Dates and Status

Oct 05, 2016

Oct 05, 2026