Taiwan FDA registration 2d77ba1571461f0766db7ea8ae80a4e8

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

TW: “富旺”非交流電力式病患升降機(未滅菌)

Taiwan·Risk Class 1·APEX HEALTH CARE MFG., INC.·Registered Nov 15, 2012 – Nov 15, 2022Cancelled

Registration details

Analysis ID: 2d77ba1571461f0766db7ea8ae80a4e8

Company information

Manufacturer: APEX HEALTH CARE MFG., INC.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: FU WONG MEDICAL 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): J.5510 Non-AC electric patient lifts
Import Information: Contract manufacturing;; Domestic

Dates and status

Registration Date: Nov 15, 2012
Expiry Date: Nov 15, 2022
Cancellation Date: Apr 12, 2024

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Fuwang" 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 2d77ba1571461f0766db7ea8ae80a4e8 and manufactured by APEX HEALTH CARE MFG., INC.. The authorized representative in Taiwan is FU WONG MEDICAL CO., LTD..

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