Taiwan FDA registration 5bea350dbf5ead2244dc0778ee344b42

"Large and medium" waste liquid collector (unsterilized)

TW: "大中"廢液收集器(未滅菌)

Taiwan·Risk Class 1·DA CHUNG MEDICAL CO., LTD.·Registered Mar 21, 2011 – Mar 21, 2016Cancelled

Registration details

Analysis ID: 5bea350dbf5ead2244dc0778ee344b42

Company information

Manufacturer: DA CHUNG MEDICAL CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: DA CHUNG MEDICAL CO., LTD.

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: Mar 21, 2011
Expiry Date: Mar 21, 2016
Cancellation Date: Aug 14, 2018

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Large and medium" waste liquid collector (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5bea350dbf5ead2244dc0778ee344b42 and manufactured by DA CHUNG MEDICAL CO., LTD.. The authorized representative in Taiwan is DA CHUNG MEDICAL CO., LTD..

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