Taiwan FDA registration 33055768dc593533703fcece2450e138
"Gufeng" manual patient turnover bed (unsterilized)
TW: “固鋒”手動式病人翻身床(未滅菌)
Taiwan·Risk Class 1·Gufeng Instrument Co., Ltd. Xinzhuang factory·Registered May 05, 2009 – May 05, 2014CancelledRegistration details
- Analysis ID
- 33055768dc593533703fcece2450e138
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 of identification scope of the "Manual Patient Turning Bed (O.5180)" for the Administrative Measures for Medical Equipment.
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.5180 手動式病人翻身床
- 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" manual patient turnover 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 33055768dc593533703fcece2450e138 and manufactured by Gufeng Instrument Co., Ltd. Xinzhuang factory. The authorized representative in Taiwan is TYMED INSTRUMENTS COMPANY.
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