Taiwan FDA registration 863271c96e6b8106f87cabd21ee880e7

"KEISEI" Dermatome (Non-Sterile)

TW: "京成" 取皮機 (未滅菌)

Taiwan·Risk Class 1·MD·KEISEI MEDICAL INDUSTRIAL CO., LTD·Registered Jan 26, 2016 – Jan 26, 2021Expired

Registration details

Analysis ID: 863271c96e6b8106f87cabd21ee880e7
License Form: Ministry of Health Medical Device Import No. 016119
Customs Code: DHA09401611908

Company information

Manufacturer: KEISEI MEDICAL INDUSTRIAL CO., LTD
Manufacturer Country: Japan
Authorized Representative: CHIUYU MEDICAL 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 26, 2016
Expiry Date: Jan 26, 2021

About this record

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..

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.