Taiwan FDA registration ae8e48596be310238b7aec2da331f9af

"DAEJU" Manual surgical instrument for general use (Non-sterile)

TW: "太宇" 一般手術用手動式器械 (未滅菌)

Taiwan·Risk Class 1·MD·DAE-JU MEDITECH ENGINEERING.·Registered May 30, 2016 – May 30, 2021Expired

Registration details

Analysis ID: ae8e48596be310238b7aec2da331f9af
License Form: Ministry of Health Medical Device Import No. 016593
Customs Code: DHA09401659300

Company information

Manufacturer: DAE-JU MEDITECH ENGINEERING.
Manufacturer Country: Korea, Republic of
Authorized Representative: YUNGLIN BIOTECHNOLOGY 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: May 30, 2016
Expiry Date: May 30, 2021

About this record

Access comprehensive regulatory information for "DAEJU" 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 ae8e48596be310238b7aec2da331f9af and manufactured by DAE-JU MEDITECH ENGINEERING.. The authorized representative in Taiwan is YUNGLIN BIOTECHNOLOGY CO., LTD..

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