Taiwan FDA registration ec7865591a75a33b691125fa0b4c8c04

"Proway" non-powered, single-patient, portable aspiration device (unsterilized)

TW: "普威" 非動力式，單一病人使用，可攜帶式之抽吸器具 (未滅菌)

Taiwan·Risk Class 1·Puwei International Co., Ltd. Taishan Factory·Registered Aug 16, 2011 – Aug 16, 2021Cancelled

Registration details

Analysis ID: ec7865591a75a33b691125fa0b4c8c04

Company information

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

Product details

Intended Use: Limited to the first level of identification scope of "non-powered, single-patient, portable suction device (I.4680)" under the Measures for the Administration of Medical Devices.
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4680 Non-motive, single patient-use, carry-on suctioning device
Import Information: Domestic

Dates and status

Registration Date: Aug 16, 2011
Expiry Date: Aug 16, 2021
Cancellation Date: Sep 08, 2023

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for "Proway" non-powered, single-patient, portable aspiration device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ec7865591a75a33b691125fa0b4c8c04 and manufactured by Puwei International Co., Ltd. Taishan Factory. The authorized representative in Taiwan is UNIMAX MEDICAL SYSTEMS INC..

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