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"Cardina" wound drainage device (unsterilized) - Taiwan Registration 51f63a717c7e682cf6f518c5ccb271e9

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.

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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51f63a717c7e682cf6f518c5ccb271e9
Registration Details
Taiwan FDA Registration: 51f63a717c7e682cf6f518c5ccb271e9
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Device Details

"Cardina" wound drainage device (unsterilized)
TW: "ๅก่ฟช็ด" ๅ‚ทๅฃๅผ•ๆต่ฃ็ฝฎ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

51f63a717c7e682cf6f518c5ccb271e9

DHA04400727107

Company Information

United States

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

import

Dates and Status

Nov 25, 2008

Nov 25, 2013

Aug 10, 2015

Cancellation Information

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