"Siemens" X-ray diagnostic system - Taiwan Registration 806649eada1aa97d96524f48d9bde6d6

Access comprehensive regulatory information for "Siemens" X-ray diagnostic system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 806649eada1aa97d96524f48d9bde6d6 and manufactured by SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD.;; SIEMENS AG, MEDICAL SOLUTIONS, BUSINESS UNIT AX. The authorized representative in Taiwan is SIEMENS LIMITED.

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD., SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD.;; Siemens Healthcare GmbH, X-Ray Products (XP), and 3 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.

Free Database

89,000+ Devices

3 Competitors

3 Recent Registrations

806649eada1aa97d96524f48d9bde6d6

Registration Details

Taiwan FDA Registration: 806649eada1aa97d96524f48d9bde6d6

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Siemens" X-ray diagnostic system

TW: “西門子” X光診斷系統

Risk Class 2

Cancelled

Registration Details

Analysis ID

806649eada1aa97d96524f48d9bde6d6

Customs Code

DHAS4200026508

Product Details

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.1750 Computed tomography X-ray system;; P.1620 Continuous or intermittent fluoroscopic X-ray machine

Import Information

Input;; Chinese goods;; Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); Contract manufacturing;; The use of this device shall comply with the provisions of the Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing.