Taiwan FDA registration 5f9b2ee0e5957edc60f006d934146cc1
"Goodman" patient lift (unsterilized)
TW: “古德曼”病患移位升降機(未滅菌)
Taiwan·Risk Class 1·V. GULDMANN A/S·Registered Aug 10, 2007 – Aug 10, 2017CancelledRegistration details
- Analysis ID
- 5f9b2ee0e5957edc60f006d934146cc1
- Customs Code
- DHA04400608008
Company information
- Manufacturer
- V. GULDMANN A/S
- Manufacturer Country
- Denmark
- Authorized Representative
- FUROTO MEDICAL & WELFARE CO., 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
- Aug 10, 2007
- Expiry Date
- Aug 10, 2017
- Cancellation Date
- Nov 26, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Goodman" 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 5f9b2ee0e5957edc60f006d934146cc1 and manufactured by V. GULDMANN A/S. The authorized representative in Taiwan is FUROTO MEDICAL & WELFARE CO., LTD..
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