Taiwan FDA registration 9770e7afb166a4f021ea7655bce99389

"Prowei" manual instruments for general surgery (unsterilized)

TW: "普威"一般手術用手動式器械(未滅菌)

Taiwan·Risk Class 1·Puwei International Co., Ltd. Yilan Factory·Registered Apr 24, 2015 – Apr 24, 2025Expired

Registration details

Analysis ID: 9770e7afb166a4f021ea7655bce99389

Company information

Manufacturer: Puwei International Co., Ltd. Yilan Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: UNIMAX MEDICAL SYSTEMS INC.

Product details

Intended Use: Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.
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: Apr 24, 2015
Expiry Date: Apr 24, 2025

About this record

Access comprehensive regulatory information for "Prowei" manual instruments for general surgery (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9770e7afb166a4f021ea7655bce99389 and manufactured by Puwei International Co., Ltd. Yilan Factory. The authorized representative in Taiwan is UNIMAX MEDICAL SYSTEMS INC..

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