Taiwan FDA registration 0a8fdbc7413097bc809c275899efba42
"Ergolet" Non-AC-powered patient lift (Non-Sterile)
TW: "愛朵樂" 非交流電力式病患升降機 (未滅菌)
Taiwan·Risk Class 1·MD·ERGOLET·Registered Nov 29, 2016 – Nov 29, 2021ExpiredRegistration details
- Analysis ID
- 0a8fdbc7413097bc809c275899efba42
- License Form
- Ministry of Health Medical Device Import No. 017223
- Customs Code
- DHA09401722308
Company information
- Manufacturer
- ERGOLET
- Manufacturer Country
- Denmark
- Authorized Representative
- HABITZ MEDTECH 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)
- J5510 Non-AC Electric Patient Lift
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 29, 2016
- Expiry Date
- Nov 29, 2021
About this record
Access comprehensive regulatory information for "Ergolet" 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 0a8fdbc7413097bc809c275899efba42 and manufactured by ERGOLET. The authorized representative in Taiwan is HABITZ MEDTECH CO., LTD..
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