Taiwan FDA registration ed35999db6ffc214d6d7255160dbd2b5

"Dense" probe hair remover (unsterilized)

TW: ”密” 探針式除毛機(未滅菌)

Taiwan·Risk Class 1·ME MEDICAL AG;; SHANGHAI POVOS ELECTRIC WORKS CO., LTD.·Registered Feb 05, 2021 – Feb 05, 2026Expired

Registration details

Analysis ID: ed35999db6ffc214d6d7255160dbd2b5
Customs Code: DHA09600443900

Company information

Manufacturer: ME MEDICAL AG;; SHANGHAI POVOS ELECTRIC WORKS CO., LTD.
Manufacturer Country: Switzerland;;China
Authorized Representative: FRIENDS SCIENTIFIC CO., LTD.

Product details

Intended Use: Limited to the first level of identification scope of the "Probe Hair Removal Machine (I.5350)" of the Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.5350 Probe type depilator
Import Information: Contract manufacturing;; Input;; Chinese goods

Dates and status

Registration Date: Feb 05, 2021
Expiry Date: Feb 05, 2026

About this record

Access comprehensive regulatory information for "Dense" probe hair remover (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ed35999db6ffc214d6d7255160dbd2b5 and manufactured by ME MEDICAL AG;; SHANGHAI POVOS ELECTRIC WORKS CO., LTD.. The authorized representative in Taiwan is FRIENDS SCIENTIFIC CO., LTD..

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