Taiwan FDA registration 1c8d34bce7de7f73b31165877dbffefd

“AESMED” Automatic Biofibre Hair Device (Non-Sterile)

TW: 髮來麗植髮機(未滅菌)

Taiwan·Risk Class 1·MD·MEDICAP S.R.L.·Registered Jan 21, 2021 – Jan 21, 2026Expired

Registration details

Analysis ID: 1c8d34bce7de7f73b31165877dbffefd
License Form: Ministry of Health Medical Device Import No. 022265
Customs Code: DHA09402226505

Company information

Manufacturer: MEDICAP S.R.L.
Manufacturer Country: Italy
Authorized Representative: AESMED CO., LTD.

Product details

Intended Use: Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Surgical Instruments, Motors and Accessories or Accessories (I.4820)".
Product Type (Level 1): I General and plastic surgical devices
Product Type (Level 2): I4820 Surgical Appliance Motors with Accessories or Accessories
Import Information: Imported from abroad

Dates and status

Registration Date: Jan 21, 2021
Expiry Date: Jan 21, 2026

About this record

Access comprehensive regulatory information for “AESMED” Automatic Biofibre Hair Device (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 1c8d34bce7de7f73b31165877dbffefd and manufactured by MEDICAP S.R.L.. The authorized representative in Taiwan is AESMED CO., LTD..

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