Taiwan FDA registration a9f8714a3754b6adb6250e3ea75b8aa9

"Manuco" non-AC electric patient lift (unsterilized)

TW: "曼紐科" 非交流電力式病患升降機 (未滅菌)

Taiwan·Risk Class 1·HUMANEOTEC HEALTH INDUSTRY (GUANGZHOU) CO., LTD·Registered Apr 13, 2017 – Apr 13, 2027Active

Registration details

Analysis ID: a9f8714a3754b6adb6250e3ea75b8aa9
Customs Code: DHA09600305401

Company information

Manufacturer: HUMANEOTEC HEALTH INDUSTRY (GUANGZHOU) CO., LTD
Manufacturer Country: China
Authorized Representative: CONTINUOUS INSTRUMENT 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: Apr 13, 2017
Expiry Date: Apr 13, 2027

About this record

Access comprehensive regulatory information for "Manuco" 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 a9f8714a3754b6adb6250e3ea75b8aa9 and manufactured by HUMANEOTEC HEALTH INDUSTRY (GUANGZHOU) CO., LTD. The authorized representative in Taiwan is CONTINUOUS INSTRUMENT CO., LTD..

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