Taiwan FDA registration 9bdf1e1bd3d8052840451a4189f33257
"Unate" bath bed (unsterilized)
TW: “優耐特”沐浴床 (未滅菌)
Taiwan·Risk Class 1·Dayi Medical Instrument Factory·Registered Dec 14, 2009 – Dec 14, 2014CancelledRegistration details
- Analysis ID
- 9bdf1e1bd3d8052840451a4189f33257
Company information
- Manufacturer
- Dayi Medical Instrument Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Dayi Medical Instrument Factory
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Non-AC Electric Patient Lift (J.5510)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5510 Non-AC electric patient lifts
- Import Information
- Domestic
Dates and status
- Registration Date
- Dec 14, 2009
- Expiry Date
- Dec 14, 2014
- Cancellation Date
- May 21, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Unate" bath 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 9bdf1e1bd3d8052840451a4189f33257 and manufactured by Dayi Medical Instrument Factory. The authorized representative in Taiwan is Dayi Medical Instrument Factory.
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