Taiwan FDA registration c3f2efd914a35eb2854a126bc14480b6

"Seto" manual instrument for general surgery (not sterilized)

TW: "世亨"一般手術用手動式器械(未滅菌)

Taiwan·Risk Class 1·SHI HENG TECHNOLOGY CO., LTD.·Registered Jan 12, 2012 – Jan 12, 2017Cancelled

Registration details

Analysis ID: c3f2efd914a35eb2854a126bc14480b6

Company information

Manufacturer: SHI HENG TECHNOLOGY CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: SHI HENG TECHNOLOGY 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, Plastic Surgery and Dermatology
Product Type (Level 2): I.4800 Hand Instruments for General Surgery
Import Information: Domestic

Dates and status

Registration Date: Jan 12, 2012
Expiry Date: Jan 12, 2017
Cancellation Date: Dec 13, 2019

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Seto" manual instrument for general surgery (not sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c3f2efd914a35eb2854a126bc14480b6 and manufactured by SHI HENG TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is SHI HENG TECHNOLOGY CO., LTD..

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