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"Cardino" wound drainage device (sterilization) - Taiwan Registration f015ab31bc63f88070c2d507e50bdad6

Access comprehensive regulatory information for "Cardino" wound drainage device (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f015ab31bc63f88070c2d507e50bdad6 and manufactured by CARDINAL HEALTH P.R. 218, INC.. The authorized representative in Taiwan is BENQ MEDICAL TECHNOLOGY CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including CARDINAL HEALTH, INC., and 2 recent registrations in the same category. 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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f015ab31bc63f88070c2d507e50bdad6
Registration Details
Taiwan FDA Registration: f015ab31bc63f88070c2d507e50bdad6
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Device Details

"Cardino" wound drainage device (sterilization)
TW: "ๅก่ฟช่ซพ" ๅ‚ทๅฃๅผ•ๆต่ฃ็ฝฎ (ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

f015ab31bc63f88070c2d507e50bdad6

DHA09401548808

Company Information

Puerto Rico

Product Details

Limited to the scope of Grade 1 identification of "Introduction/Drainage Catheters and Their Accessories (I.4200)" under the Measures for the Administration of Medical Devices.

I General, Plastic Surgery and Dermatology

I.4200 Incoming/Drainage Tubes and Accessories

Input;; QMS/QSD

Dates and Status

Jul 21, 2015

Jul 21, 2020

Jun 16, 2022

Cancellation Information

Logged out

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