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"Elecon" wound drainage device (sterilization) - Taiwan Registration 7a2c013e0e365be8948f096156290752

Access comprehensive regulatory information for "Elecon" 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 7a2c013e0e365be8948f096156290752 and manufactured by ALCARE CO., LTD., CHIBA FACTORY WEST. The authorized representative in Taiwan is HORIZON INSTRUMENTS 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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7a2c013e0e365be8948f096156290752
Registration Details
Taiwan FDA Registration: 7a2c013e0e365be8948f096156290752
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Device Details

"Elecon" wound drainage device (sterilization)
TW: โ€œๆ„›ๆจ‚ๅบทโ€ๅ‚ทๅฃๅผ•ๆต่ฃ็ฝฎ(ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

7a2c013e0e365be8948f096156290752

DHA04400937503

Company Information

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

Oct 14, 2010

Oct 14, 2020

Jun 07, 2022

Cancellation Information

Logged out

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