Taiwan FDA registration 0620c798ec7dba7e4e03976b3552833f
"Gufeng" non-powered treatment mattress (unsterilized)
TW: “固鋒”非動力式治療床墊 (未滅菌)
Taiwan·Risk Class 1·Gufeng Instrument Co., Ltd. Xinzhuang factory·Registered May 05, 2009 – May 05, 2014CancelledRegistration details
- Analysis ID
- 0620c798ec7dba7e4e03976b3552833f
Company information
- Manufacturer
- Gufeng Instrument Co., Ltd. Xinzhuang factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- TYMED INSTRUMENTS COMPANY
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
Dates and status
- Registration Date
- May 05, 2009
- Expiry Date
- May 05, 2014
- Cancellation Date
- Dec 14, 2016
Cancellation information
- Status
- Logged out
- Reason
- 屆期未申請展延
About this record
Access comprehensive regulatory information for "Gufeng" 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 0620c798ec7dba7e4e03976b3552833f and manufactured by Gufeng Instrument Co., Ltd. Xinzhuang factory. The authorized representative in Taiwan is TYMED INSTRUMENTS COMPANY.
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