Pure Global

"Siemens" diagnostic X-ray machine - Taiwan Registration 8fc52cd492e213a495dd85d5efe84781

Access comprehensive regulatory information for "Siemens" diagnostic X-ray machine in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8fc52cd492e213a495dd85d5efe84781 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 AG, MEDICAL SOLUTIONS, BUSINESS UNIT XP, Siemens Healthcare GmbH, X-Ray Products (XP), and 4 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
Powered by Pure Global AI
89,000+ Devices
3 Competitors
4 Recent Registrations
8fc52cd492e213a495dd85d5efe84781
Registration Details
Taiwan FDA Registration: 8fc52cd492e213a495dd85d5efe84781
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Siemens" diagnostic X-ray machine
TW: โ€œ่ฅฟ้–€ๅญโ€่จบๆ–ทๅž‹Xๅ…‰ๆฉŸ
Risk Class 2
Cancelled

Registration Details

8fc52cd492e213a495dd85d5efe84781

DHAS4200040804

Company Information

Product Details

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

P Radiology Science

P.1680 ๅ›บๅฎšๅผXๅ…‰็ณป็ตฑ

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

Dec 19, 2011

Dec 19, 2016

Jul 31, 2018

Cancellation Information

Logged out

ๆœชๅฑ•ๅปถ่€Œ้€พๆœŸ่€