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Mobile X-ray system "Siemens" - Taiwan Registration 17116ab5622167e2173b77cfc5fcf91f

Access comprehensive regulatory information for Mobile X-ray system "Siemens" in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 17116ab5622167e2173b77cfc5fcf91f and manufactured by Siemens Healthcare GmbH;; SIEMENS SHANGHAI MEDICAL EQUIPMENT 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 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.

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17116ab5622167e2173b77cfc5fcf91f
Registration Details
Taiwan FDA Registration: 17116ab5622167e2173b77cfc5fcf91f
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Device Details

Mobile X-ray system "Siemens"
TW: โ€œ่ฅฟ้–€ๅญโ€็งปๅ‹•ๅผXๅ…‰็ณป็ตฑ
Risk Class 2

Registration Details

17116ab5622167e2173b77cfc5fcf91f

DHAS9200083401

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

P Radiology Science

P.1730 ็…ง็›ธ้€่ฆ–Xๅ…‰็ณป็ตฑ

Input;; Chinese goods;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)

Dates and Status

May 15, 2017

May 15, 2027