Taiwan FDA registration 951f36b4d06aece24885dd7cb90053b2

Ruidaton powered airflow floating treatment bed (unsterilized)

TW: “瑞達通”動力式氣流漂浮治療床 (未滅菌)

Taiwan·Risk Class 1·REDACTRON INTERNATIONAL B.V.·Registered Jul 22, 2010 – Jul 22, 2015Cancelled

Registration details

Analysis ID: 951f36b4d06aece24885dd7cb90053b2
Customs Code: DHA04400899900

Company information

Manufacturer: REDACTRON INTERNATIONAL B.V.
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 Physical Medical Sciences
Product Type (Level 2): O.5170 5170.
Import Information: import

Dates and status

Registration Date: Jul 22, 2010
Expiry Date: Jul 22, 2015
Cancellation Date: Apr 25, 2018

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for Ruidaton powered airflow floating treatment bed (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 951f36b4d06aece24885dd7cb90053b2 and manufactured by REDACTRON INTERNATIONAL B.V.. The authorized representative in Taiwan is MEDITECHS INSTRUMENTS CO., LTD..

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