Taiwan FDA registration 0c6e435e56b3c6388e56f8bccfebd081

"Livehold" waste collection bag (unsterilized)

TW: "活岳" 廢液收集袋 (未滅菌)

Taiwan·Risk Class 1·Amedifact Co., Ltd.·Registered Jul 09, 2018 – Jul 09, 2028Active

Registration details

Analysis ID: 0c6e435e56b3c6388e56f8bccfebd081

Company information

Manufacturer: Amedifact Co., Ltd.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: SUNPHORIA CO., LTD.

Product details

Intended Use: Limited to the first level of classification and grading management of medical equipment, "Non-powered, single-patient, portable suction equipment (I.4680)".
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;; Contract manufacturing

Dates and status

Registration Date: Jul 09, 2018
Expiry Date: Jul 09, 2028

About this record

Access comprehensive regulatory information for "Livehold" waste collection bag (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0c6e435e56b3c6388e56f8bccfebd081 and manufactured by Amedifact Co., Ltd.. The authorized representative in Taiwan is SUNPHORIA CO., LTD..

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