Taiwan FDA registration f43176daf0753081deb7027df4d63095
"Revitalizing" non-powered treatment mattress (unsterilized)
TW: "元氣活現" 非動力式治療床墊 (未滅菌)
Registration details
- Analysis ID
- f43176daf0753081deb7027df4d63095
Company information
- Manufacturer
- Chengyou An Technology Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- IDTREND CORPORATION
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-powered Therapeutic Mattresses (J.5150)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5150 Non-powered floating therapy mattress
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Jan 02, 2014
- Expiry Date
- Jan 02, 2019
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Revitalizing" non-powered treatment mattress (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f43176daf0753081deb7027df4d63095 and manufactured by Chengyou An Technology Co., Ltd. The authorized representative in Taiwan is IDTREND CORPORATION.
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.
Free DatabasePowered by Pure Global AI89,000+ Devices