Taiwan FDA registration b562f957a74a61532eec1948dc3aba03

"KEISEI" Powered flotation therapy bed (Non-Sterile)

TW: "京成" 動力式氣流漂浮治療床 (未滅菌)

Taiwan·Risk Class 1·MD·KEISEI MEDICAL INDUSTRIAL CO., LTD·Registered Oct 05, 2016 – Oct 05, 2026Active

Registration details

Analysis ID: b562f957a74a61532eec1948dc3aba03
License Form: Ministry of Health Medical Device Import No. 017055
Customs Code: DHA09401705500

Company information

Manufacturer: KEISEI MEDICAL INDUSTRIAL CO., LTD
Manufacturer Country: Japan
Authorized Representative: CHIUYU MEDICAL CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Powered Airflow Floating Treatment Bed (O.5170)".
Product Type (Level 1): o Equipment for physical medicine
Product Type (Level 2): O5170 powered airflow floating treatment bed
Import Information: Imported from abroad

Dates and status

Registration Date: Oct 05, 2016
Expiry Date: Oct 05, 2026

About this record

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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