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"KEISEI" Dermatome (Non-Sterile) - Taiwan Registration 863271c96e6b8106f87cabd21ee880e7

Access comprehensive regulatory information for "KEISEI" Dermatome (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 863271c96e6b8106f87cabd21ee880e7 and manufactured by KEISEI MEDICAL INDUSTRIAL CO., LTD. The authorized representative in Taiwan is CHIUYU MEDICAL CO., LTD..

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863271c96e6b8106f87cabd21ee880e7
Registration Details
Taiwan FDA Registration: 863271c96e6b8106f87cabd21ee880e7
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Device Details

"KEISEI" Dermatome (Non-Sterile)
TW: "ไบฌๆˆ" ๅ–็šฎๆฉŸ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

863271c96e6b8106f87cabd21ee880e7

Ministry of Health Medical Device Import No. 016119

DHA09401611908

Company Information

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 26, 2016

Jan 26, 2021