Radiology Patient Stent (Unsterilized)
- Analysis ID
- b1ed666628e73083de844b2b549c5793
- Customs Code
- DHA04400787401
- Manufacturer
- WFR/ AQUAPLAST CORP. AND Q-FIX SYSTEMS, LLC
- Manufacturer Country
- United States
- Authorized Representative
- Shengtaihe Limited
- 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
- Registration Date
- Jul 02, 2009
- Expiry Date
- Jul 02, 2014
- Cancellation Date
- Apr 25, 2018
- Status
- Logged out
- Reason
- 自行鍵入
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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.