Taiwan FDA registration 51f63a717c7e682cf6f518c5ccb271e9

"Cardina" wound drainage device (unsterilized)

TW: "卡迪納" 傷口引流裝置(未滅菌)

Taiwan·Risk Class 1·CARDINAL HEALTH, INC.·Registered Nov 25, 2008 – Nov 25, 2013Cancelled

Registration details

Analysis ID: 51f63a717c7e682cf6f518c5ccb271e9
Customs Code: DHA04400727107

Company information

Manufacturer: CARDINAL HEALTH, INC.
Manufacturer Country: United States
Authorized Representative: CHAMPION MEDICAL CORPORATION

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: import

Dates and status

Registration Date: Nov 25, 2008
Expiry Date: Nov 25, 2013
Cancellation Date: Aug 10, 2015

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for "Cardina" wound drainage 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 51f63a717c7e682cf6f518c5ccb271e9 and manufactured by CARDINAL HEALTH, INC.. The authorized representative in Taiwan is CHAMPION MEDICAL CORPORATION.

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