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“AESMED” Automatic Biofibre Hair Device (Non-Sterile) - Taiwan Registration 1c8d34bce7de7f73b31165877dbffefd

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..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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1c8d34bce7de7f73b31165877dbffefd
Registration Details
Taiwan FDA Registration: 1c8d34bce7de7f73b31165877dbffefd
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Device Details

“AESMED” Automatic Biofibre Hair Device (Non-Sterile)
TW: 髮來麗植髮機(未滅菌)
Risk Class 1
MD

Registration Details

1c8d34bce7de7f73b31165877dbffefd

Ministry of Health Medical Device Import No. 022265

DHA09402226505

Company Information

Italy

Product Details

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)".

I General and plastic surgical devices

I4820 Surgical Appliance Motors with Accessories or Accessories

Imported from abroad

Dates and Status

Jan 21, 2021

Jan 21, 2026