Taiwan FDA registration b1ed666628e73083de844b2b549c5793

Radiology Patient Stent (Unsterilized)

TW: “巧福思”放射科病患用支架 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·WFR/ AQUAPLAST CORP. AND Q-FIX SYSTEMS, LLC·Registered Jul 02, 2009 – Jul 02, 2014Cancelled
Registration details
Analysis ID
b1ed666628e73083de844b2b549c5793
Customs Code
DHA04400787401
Company information
Manufacturer Country
United States
Authorized Representative
Shengtaihe Limited
Product details
Intended Use
Limited to the first-level identification range of the Measures for the Administration of Medical Equipment "Stent 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
import
Dates and status
Registration Date
Jul 02, 2009
Expiry Date
Jul 02, 2014
Cancellation Date
Apr 25, 2018
Cancellation information
Status
Logged out
Reason
自行鍵入
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About this record

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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