Taiwan FDA registration 965e6bcef31b4115c95036fdf2ac0c6b

"KEISEI" Manual surgical instrument for general use (Non-Sterile)

TW: "京成" 一般手術用手動式器械 (未滅菌)

Taiwan·Risk Class 1·MD·KEISEI MEDICAL INDUSTRIAL CO., LTD·Registered Oct 05, 2016 – Oct 05, 2021Expired

Registration details

Analysis ID: 965e6bcef31b4115c95036fdf2ac0c6b
License Form: Ministry of Health Medical Device Import No. 017056
Customs Code: DHA09401705602

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 identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
Product Type (Level 1): I General and plastic surgical devices
Product Type (Level 2): I4800 General Surgery Manual Instrument
Import Information: Imported from abroad

Dates and status

Registration Date: Oct 05, 2016
Expiry Date: Oct 05, 2021

About this record

Access comprehensive regulatory information for "KEISEI" Manual surgical instrument for general use (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 965e6bcef31b4115c95036fdf2ac0c6b 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.