Taiwan FDA registration 3905013e162bf15b99864f54f887aace

"Siemens" angiography system

TW: “西門子"血管攝影系統
Taiwan flagTaiwan·Risk Class 2·Siemens Healthineers AG, Advanced Therapies·Registered Mar 15, 2022 – Mar 15, 2027Active
Registration details
Analysis ID
3905013e162bf15b99864f54f887aace
Customs Code
DHAS5603532901
Company information
Manufacturer Country
Germany
Authorized Representative
SIEMENS HEALTHCARE LIMITED
Product details
Intended Use
Details are as detailed as approved Chinese instructions
Product Type (Level 1)
P Radiology Science
Product Type (Level 2)
P.1600 X光血管攝影系統
Import Information
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
Registration Date
Mar 15, 2022
Expiry Date
Mar 15, 2027
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About this record

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 3905013e162bf15b99864f54f887aace and manufactured by Siemens Healthineers AG, 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 Healthcare GmbH, Advanced Therapies, 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.

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