Taiwan FDA registration 504046e2d3e28a36410f24db95fd38ab
"Prince" powered therapy unit (unsterilized)
TW: “普林斯”動力式治療檯 (未滅菌)
Registration details
- Analysis ID
- 504046e2d3e28a36410f24db95fd38ab
- Customs Code
- DHA04400729001
Company information
- Manufacturer
- PLINTH 2000 LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- Yuanhong Instrument Co., Ltd
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Powered Treatment Units (O.3760)".
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.3760 Powered therapy cage
- Import Information
- import
Dates and status
- Registration Date
- Dec 03, 2008
- Expiry Date
- Dec 03, 2013
- Cancellation Date
- Apr 24, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Prince" powered therapy unit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 504046e2d3e28a36410f24db95fd38ab and manufactured by PLINTH 2000 LTD.. The authorized representative in Taiwan is Yuanhong Instrument Co., Ltd.
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