Taiwan FDA registration 092cb16ca7fdba0a62496fc26c2aab5e
"Ruidato" powered airflow floating treatment bed
TW: "瑞達通"動力式氣流飄浮治療床
Registration details
- Analysis ID
- 092cb16ca7fdba0a62496fc26c2aab5e
- Customs Code
- DHA04400238408
Company information
- Manufacturer
- REDACTRON INTERNATIONAL B.V.
- Manufacturer Country
- Netherlands
- Authorized Representative
- MEDITECHS INSTRUMENTS CO., LTD.
Product details
- Intended Use
- It treats bedsores, burns and helps blood circulation.
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.5170 5170.
- Import Information
- import
Dates and status
- Registration Date
- Dec 28, 2005
- Expiry Date
- Dec 28, 2010
- Cancellation Date
- Apr 30, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Ruidato" powered airflow floating treatment bed in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 092cb16ca7fdba0a62496fc26c2aab5e and manufactured by REDACTRON INTERNATIONAL B.V.. The authorized representative in Taiwan is MEDITECHS INSTRUMENTS CO., LTD..
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