Taiwan FDA registration 30bcf64c7529c84ab92075700e9866ce

“I KEN” Suture Needles (Non-Sterile)

TW: “醫研”醫療用縫合針 (未滅菌)

Taiwan·Risk Class 1·MD·I KEN KOGYO CO., LTD.·Registered Dec 26, 2013 – Dec 26, 2023Expired

Registration details

Analysis ID: 30bcf64c7529c84ab92075700e9866ce
License Form: Ministry of Health Medical Device Import No. 013727
Customs Code: DHA09401372703

Company information

Manufacturer: I KEN KOGYO CO., LTD.
Manufacturer Country: Japan
Authorized Representative: LAIFA 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: Dec 26, 2013
Expiry Date: Dec 26, 2023

About this record

Access comprehensive regulatory information for “I KEN” Suture Needles (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 30bcf64c7529c84ab92075700e9866ce and manufactured by I KEN KOGYO CO., LTD.. The authorized representative in Taiwan is LAIFA CO., LTD..

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