Taiwan FDA registration a6b42f038b46dc7ef4f53931d3db8076
"Guldmann" Patient Lift (Non-Sterile)
TW: "古曼" 病患移位升降機 (未滅菌)
Taiwan·Risk Class 1·MD·V. GULDMANN A/S·Registered Mar 07, 2014 – Mar 07, 2024ExpiredRegistration details
- Analysis ID
- a6b42f038b46dc7ef4f53931d3db8076
- License Form
- Ministry of Health Medical Device Import No. 013922
- Customs Code
- DHA09401392201
Company information
- Manufacturer
- V. GULDMANN A/S
- Manufacturer Country
- Denmark
- Authorized Representative
- ABILITIES HEALTHCARE INCORPORATED
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)
- J5510 Non-AC Electric Patient Lift
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 07, 2014
- Expiry Date
- Mar 07, 2024
About this record
Access comprehensive regulatory information for "Guldmann" Patient Lift (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a6b42f038b46dc7ef4f53931d3db8076 and manufactured by V. GULDMANN A/S. The authorized representative in Taiwan is ABILITIES HEALTHCARE INCORPORATED.
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