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"Siemens" X-ray vascular diagnostic system - Taiwan Registration ddb353d343cb89fdb94d4ebe8218d332

Access comprehensive regulatory information for "Siemens" X-ray vascular 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 ddb353d343cb89fdb94d4ebe8218d332 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, 1 companies making similar products including SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD., and 1 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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ddb353d343cb89fdb94d4ebe8218d332
Registration Details
Taiwan FDA Registration: ddb353d343cb89fdb94d4ebe8218d332
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Device Details

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

Registration Details

ddb353d343cb89fdb94d4ebe8218d332

DHAS4200014001

Company Information

Product Details

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

P Radiology Science

P.1600 Xๅ…‰่ก€็ฎกๆ”ๅฝฑ็ณป็ตฑ

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

Dates and Status

Sep 04, 2006

Sep 04, 2016

Jul 31, 2018

Cancellation Information

Logged out

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