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"SYNERGIE" Powered flotation therapy bed (Non-Sterile) - Taiwan Registration ee626f03d45b75efdc44fa35f138f000

Access comprehensive regulatory information for "SYNERGIE" 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 ee626f03d45b75efdc44fa35f138f000 and manufactured by SYNERGIE NEDERLAND BV. The authorized representative in Taiwan is MEDITECHS INSTRUMENTS CO., LTD..

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ee626f03d45b75efdc44fa35f138f000
Registration Details
Taiwan FDA Registration: ee626f03d45b75efdc44fa35f138f000
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Device Details

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

Registration Details

ee626f03d45b75efdc44fa35f138f000

Ministry of Health Medical Device Import No. 015723

DHA09401572305

Company Information

Netherlands

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 07, 2015

Oct 07, 2025