Taiwan FDA registration c156c9f16a217ac7ec891d14108465d0

"Yaoxin" non-powered, single patient, portable suction device (unsterilized)

TW: “耀信”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·Dry Biomedical Technology Co., Ltd. Forest Factory·Registered Feb 23, 2010 – Feb 23, 2015Cancelled

Registration details

Analysis ID: c156c9f16a217ac7ec891d14108465d0

Company information

Manufacturer: Dry Biomedical Technology Co., Ltd. Forest Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Yaoxin Medical Equipment 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;; Contract manufacturing

Dates and status

Registration Date: Feb 23, 2010
Expiry Date: Feb 23, 2015
Cancellation Date: Jun 26, 2018

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Yaoxin" non-powered, single patient, portable suction 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 c156c9f16a217ac7ec891d14108465d0 and manufactured by Dry Biomedical Technology Co., Ltd. Forest Factory. The authorized representative in Taiwan is Yaoxin Medical Equipment Co., Ltd.

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