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"Yaoxin" non-powered, single patient, portable suction device (unsterilized) - Taiwan Registration c156c9f16a217ac7ec891d14108465d0

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.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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c156c9f16a217ac7ec891d14108465d0
Registration Details
Taiwan FDA Registration: c156c9f16a217ac7ec891d14108465d0
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Device Details

"Yaoxin" non-powered, single patient, portable suction device (unsterilized)
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Risk Class 1
Cancelled

Registration Details

c156c9f16a217ac7ec891d14108465d0

Company Information

Taiwan, Province of China

Product Details

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.

I General, Plastic Surgery and Dermatology

I.4680 Non-motive, single patient-use, carry-on suctioning device

Domestic;; Contract manufacturing

Dates and Status

Feb 23, 2010

Feb 23, 2015

Jun 26, 2018

Cancellation Information

Logged out

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