Pure Global

"Siemens" angiography system - Taiwan Registration 68168349546c4b3d0f49e5939e7fb4e4

Access comprehensive regulatory information for "Siemens" angiography system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 68168349546c4b3d0f49e5939e7fb4e4 and manufactured by Siemens Healthcare GmbH, Advanced Therapies. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including Siemens Healthineers AG, Advanced Therapies, SIEMENS SHENZHEN MAGNETIC RESONANCE LTD., and 5 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
5 Recent Registrations
68168349546c4b3d0f49e5939e7fb4e4
Registration Details
Taiwan FDA Registration: 68168349546c4b3d0f49e5939e7fb4e4
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Siemens" angiography system
TW: โ€œ่ฅฟ้–€ๅญโ€ ่ก€็ฎกๆ”ๅฝฑ็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

68168349546c4b3d0f49e5939e7fb4e4

DHAS5602668509

Company Information

Product Details

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

P Radiology Science

P.1600 Xๅ…‰่ก€็ฎกๆ”ๅฝฑ็ณป็ตฑ

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

Nov 24, 2014

Nov 24, 2019

May 19, 2022

Cancellation Information

Logged out

่‡ช่กŒ้ตๅ…ฅ