Taiwan FDA registration d808fd616030b69fecb06729e7cb1bc4

"Steady Fortune" Non-AC Electric Patient Lift (Unsterilized)

TW: “穩得福” 非交流電力式病患升降機 (未滅菌)

Taiwan·Risk Class 1·SHANGHAI SHUNLONG PTE CO., LTD.·Registered Mar 19, 2019 – Mar 19, 2024Expired

Registration details

Analysis ID: d808fd616030b69fecb06729e7cb1bc4
Customs Code: DHA09600372802

Company information

Manufacturer: SHANGHAI SHUNLONG PTE CO., LTD.
Manufacturer Country: China
Authorized Representative: FUGI ASSISTIVE DEVICE CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the "Non-AC Power Patient Lift (J.5510)" of the Measures for the Classification and Grading Management of Medical Equipment.
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.5510 Non-AC electric patient lifts
Import Information: Input;; Chinese goods

Dates and status

Registration Date: Mar 19, 2019
Expiry Date: Mar 19, 2024

About this record

Access comprehensive regulatory information for "Steady Fortune" Non-AC Electric 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 d808fd616030b69fecb06729e7cb1bc4 and manufactured by SHANGHAI SHUNLONG PTE CO., LTD.. The authorized representative in Taiwan is FUGI ASSISTIVE DEVICE CO., LTD..

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