"Siemens" angiography system
Taiwan·Risk Class 2·SIEMENS SHENZHEN MAGNETIC RESONANCE LTD.·Registered Sep 10, 2014 – Sep 10, 2029Active- Analysis ID
- 34becf7a8a4042245e844426a1627c32
- Customs Code
- DHAS9200063100
- Manufacturer
- SIEMENS SHENZHEN MAGNETIC RESONANCE LTD.
- Manufacturer Country
- China
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1600 X-ray Vascular Photography System;; P.1650 Fluoroscopic X-ray Sensory Tube
- Import Information
- Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); Input;; Chinese goods
- Registration Date
- Sep 10, 2014
- Expiry Date
- Sep 10, 2029
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Access comprehensive regulatory information for "Siemens" angiography system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 34becf7a8a4042245e844426a1627c32 and manufactured by SIEMENS SHENZHEN MAGNETIC RESONANCE LTD.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Siemens Healthineers AG, Advanced Therapies, Siemens Healthcare GmbH, Advanced Therapies, 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.