Taiwan FDA registration 361a64f303bd38d85ea60fe2f658a1f3

"Alecon" Morgo Radiology Patient Stent (Non-sterilized)

TW: "愛樂康" 摩固放射科病患用支架(未滅菌)

Taiwan·Risk Class 1·ALCARE CO., LTD.·Registered Apr 11, 2024 – Apr 11, 2029Active

Registration details

Analysis ID: 361a64f303bd38d85ea60fe2f658a1f3
Customs Code: DHA09402344400

Company information

Manufacturer: ALCARE CO., LTD.
Manufacturer Country: Japan
Authorized Representative: CHIU HO MEDICAL SYSTEM CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the classification and grading management measures for medical equipment "Stents for Radiology Patients (P.1830)".
Product Type (Level 1): P Radiology Science
Product Type (Level 2): P.1830 放射科病患用支架
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: Apr 11, 2024
Expiry Date: Apr 11, 2029

About this record

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.