Taiwan FDA registration e0aeea21a847cbef5b2f9ffab948dc0b

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

TW: "瑞穗" 一般手術用手動式器械 (未滅菌)

Taiwan·Risk Class 1·MD·MIZUHO CORPORATION·Registered May 05, 2015 – May 05, 2025Expired

Registration details

Analysis ID: e0aeea21a847cbef5b2f9ffab948dc0b
License Form: Ministry of Health Medical Device Import No. 015194
Customs Code: DHA09401519404

Company information

Manufacturer: MIZUHO CORPORATION
Manufacturer Country: Japan
Authorized Representative: FU TAI TRADING 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 05, 2015
Expiry Date: May 05, 2025

About this record

Access comprehensive regulatory information for "Mizuho" 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 e0aeea21a847cbef5b2f9ffab948dc0b and manufactured by MIZUHO CORPORATION. The authorized representative in Taiwan is FU TAI TRADING CO., LTD..

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