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"Alecon" Morgo Radiology Patient Stent (Non-sterilized) - Taiwan Registration 361a64f303bd38d85ea60fe2f658a1f3

Access comprehensive regulatory information for "Alecon" Morgo Radiology Patient Stent (Non-sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 361a64f303bd38d85ea60fe2f658a1f3 and manufactured by ALCARE CO., LTD.. The authorized representative in Taiwan is CHIU HO MEDICAL SYSTEM 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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361a64f303bd38d85ea60fe2f658a1f3
Registration Details
Taiwan FDA Registration: 361a64f303bd38d85ea60fe2f658a1f3
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Device Details

"Alecon" Morgo Radiology Patient Stent (Non-sterilized)
TW: "ๆ„›ๆจ‚ๅบท" ๆ‘ฉๅ›บๆ”พๅฐ„็ง‘็—…ๆ‚ฃ็”จๆ”ฏๆžถ(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

361a64f303bd38d85ea60fe2f658a1f3

DHA09402344400

Company Information

Japan

Product Details

Limited to the first level identification range of the classification and grading management measures for medical equipment "Stents for Radiology Patients (P.1830)".

P Radiology Science

P.1830 ๆ”พๅฐ„็ง‘็—…ๆ‚ฃ็”จๆ”ฏๆžถ

Input;; QMS/QSD

Dates and Status

Apr 11, 2024

Apr 11, 2029