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"Siemens" X-ray diagnostic system - Taiwan Registration b978b07808d4166b32ad694a1293d295

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 b978b07808d4166b32ad694a1293d295 and manufactured by SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD.. 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 Healthcare GmbH, X-Ray Products (XP), SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD.;; SIEMENS AG, MEDICAL SOLUTIONS, BUSINESS UNIT AX, 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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b978b07808d4166b32ad694a1293d295
Registration Details
Taiwan FDA Registration: b978b07808d4166b32ad694a1293d295
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Device Details

"Siemens" X-ray diagnostic system
TW: "่ฅฟ้–€ๅญ"Xๅ…‰่จบๆ–ท็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

b978b07808d4166b32ad694a1293d295

DHAS4200010002

Company Information

Product Details

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

P Radiology Science

Chinese goods;; Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); input

Dates and Status

Mar 17, 2006

Mar 17, 2016

Jul 31, 2018

Cancellation Information

Logged out

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