Taiwan FDA registration e7d9260ff9e35f5ab06c65965a935234
"ROPOX" Non-AC-powered patient lift (Non-Sterile)
TW: "羅帕斯" 非交流電力式病患升降機 (未滅菌)
Registration details
- Analysis ID
- e7d9260ff9e35f5ab06c65965a935234
- License Form
- Ministry of Health Medical Device Import No. 021756
- Customs Code
- DHA09402175606
Company information
- Manufacturer
- ROPOX 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
- Jul 20, 2020
- Expiry Date
- Jul 20, 2025
About this record
Access comprehensive regulatory information for "ROPOX" 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 e7d9260ff9e35f5ab06c65965a935234 and manufactured by ROPOX A/S. The authorized representative in Taiwan is ABILITIES HEALTHCARE INCORPORATED.
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