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Radiology Patient Stent (Unsterilized) - Taiwan Registration b1ed666628e73083de844b2b549c5793

Access comprehensive regulatory information for Radiology Patient Stent (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b1ed666628e73083de844b2b549c5793 and manufactured by WFR/ AQUAPLAST CORP. AND Q-FIX SYSTEMS, LLC. The authorized representative in Taiwan is Shengtaihe Limited.

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including POSKOM CO., LTD., ANHUI AMEC INTERNATIONAL TRADE CO., LTD, and 5 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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b1ed666628e73083de844b2b549c5793
Registration Details
Taiwan FDA Registration: b1ed666628e73083de844b2b549c5793
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Device Details

Radiology Patient Stent (Unsterilized)
TW: โ€œๅทง็ฆๆ€โ€ๆ”พๅฐ„็ง‘็—…ๆ‚ฃ็”จๆ”ฏๆžถ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

b1ed666628e73083de844b2b549c5793

DHA04400787401

Company Information

Product Details

Limited to the first-level identification range of the Measures for the Administration of Medical Equipment "Stent for Radiology Patients (P.1830)".

P Radiology Science

P.1830 ๆ”พๅฐ„็ง‘็—…ๆ‚ฃ็”จๆ”ฏๆžถ

import

Dates and Status

Jul 02, 2009

Jul 02, 2014

Apr 25, 2018

Cancellation Information

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