Taiwan FDA registration 8cd0fa52698de9d2936a2059f7c46af4
"Dan Kell" non-AC electric patient lift (unsterilized)
TW: "丹凱爾" 非交流電力式病患升降機(未滅菌)
Taiwan·Risk Class 1·VANCARE INC.·Registered Jun 23, 2011 – Jun 23, 2021CancelledRegistration details
- Analysis ID
- 8cd0fa52698de9d2936a2059f7c46af4
- Customs Code
- DHA04401049908
Company information
- Manufacturer
- VANCARE INC.
- Manufacturer Country
- United States
- Authorized Representative
- FAMOUS INSTRUMENT LTD.
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
- import
Dates and status
- Registration Date
- Jun 23, 2011
- Expiry Date
- Jun 23, 2021
- Cancellation Date
- Aug 28, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Dan Kell" non-AC electric patient lift (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8cd0fa52698de9d2936a2059f7c46af4 and manufactured by VANCARE INC.. The authorized representative in Taiwan is FAMOUS INSTRUMENT LTD..
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