Taiwan FDA registration ee626f03d45b75efdc44fa35f138f000

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

TW: "信尼吉" 動力式氣流漂浮治療床 (未滅菌)

Taiwan·Risk Class 1·MD·SYNERGIE NEDERLAND BV·Registered Oct 07, 2015 – Oct 07, 2025Expired

Registration details

Analysis ID: ee626f03d45b75efdc44fa35f138f000
License Form: Ministry of Health Medical Device Import No. 015723
Customs Code: DHA09401572305

Company information

Manufacturer: SYNERGIE NEDERLAND BV
Manufacturer Country: Netherlands
Authorized Representative: MEDITECHS INSTRUMENTS 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 07, 2015
Expiry Date: Oct 07, 2025

About this record

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..

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.