Taiwan FDA registration ce4002924d084f7d479df9ad4d770ff8
"HandiMove" Non-AC-powered patient lift (Non-sterile)
TW: "漢地魔輔" 非交流電力式病患升降機 (未滅菌)
Taiwan·Risk Class 1·MD·HANDI-MOVE INTERNATIONAL·Registered Nov 15, 2016 – Nov 15, 2021ExpiredRegistration details
- Analysis ID
- ce4002924d084f7d479df9ad4d770ff8
- License Form
- Ministry of Health Medical Device Import No. 017176
- Customs Code
- DHA09401717602
Company information
- Manufacturer
- HANDI-MOVE INTERNATIONAL
- Manufacturer Country
- Belgium
- Authorized Representative
- Johnson & Johnson Medical Instruments Inc
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
- Nov 15, 2016
- Expiry Date
- Nov 15, 2021
About this record
Access comprehensive regulatory information for "HandiMove" Non-AC-powered 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 ce4002924d084f7d479df9ad4d770ff8 and manufactured by HANDI-MOVE INTERNATIONAL. The authorized representative in Taiwan is Johnson & Johnson Medical Instruments Inc.
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