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"Benoy" non-motilated, single-patient, portable aspiration device (unsterilized) - Taiwan Registration 0323bfbe5017d0229e0b4c2f6f90aea7

Access comprehensive regulatory information for "Benoy" non-motilated, single-patient, portable aspiration 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 0323bfbe5017d0229e0b4c2f6f90aea7 and manufactured by BEINUOSI MEDICAL. The authorized representative in Taiwan is ASIACONNECT INTERNATIONAL COMPANY 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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0323bfbe5017d0229e0b4c2f6f90aea7
Registration Details
Taiwan FDA Registration: 0323bfbe5017d0229e0b4c2f6f90aea7
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Device Details

"Benoy" non-motilated, single-patient, portable aspiration device (unsterilized)
TW: "่ฒ่ซพ"้žๅ‹•ๅŠ›ๅผ๏ผŒๅ–ฎไธ€็—…ไบบไฝฟ็”จ๏ผŒๅฏๆ”œๅธถๅผไน‹ๆŠฝๅธๅ™จๅ…ท(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

0323bfbe5017d0229e0b4c2f6f90aea7

DHA04600186601

Company Information

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

Chinese goods;; input

Dates and Status

Mar 28, 2013

Mar 28, 2018

Dec 20, 2019

Cancellation Information

Logged out

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