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"Cardino" vacuum wound drainage sleeve (sterilized) - Taiwan Registration 3ae69a72ead136b0e58faf6b952cf66a

Access comprehensive regulatory information for "Cardino" vacuum wound drainage sleeve (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3ae69a72ead136b0e58faf6b952cf66a 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 1 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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3ae69a72ead136b0e58faf6b952cf66a
Registration Details
Taiwan FDA Registration: 3ae69a72ead136b0e58faf6b952cf66a
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Device Details

"Cardino" vacuum wound drainage sleeve (sterilized)
TW: "ๅก่ฟช่ซพ" ็œŸ็ฉบๅ‚ทๅฃๅผ•ๆตๅฅ— (ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

3ae69a72ead136b0e58faf6b952cf66a

DHA09401618600

Company Information

Puerto Rico

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

Input;; QMS/QSD

Dates and Status

Feb 24, 2016

Feb 24, 2021

Sep 11, 2023

Cancellation Information

Logged out

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