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"Siemens" diagnostic X-ray tube sleeve assembly (unsterilized) - Taiwan Registration 2d79642e0f749d4dfbb80aa2f221e8cd

Access comprehensive regulatory information for "Siemens" diagnostic X-ray tube sleeve assembly (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2d79642e0f749d4dfbb80aa2f221e8cd 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, 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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2d79642e0f749d4dfbb80aa2f221e8cd
Registration Details
Taiwan FDA Registration: 2d79642e0f749d4dfbb80aa2f221e8cd
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Device Details

"Siemens" diagnostic X-ray tube sleeve assembly (unsterilized)
TW: "่ฅฟ้–€ๅญ" ่จบๆ–ท็”จXๅ…‰็ƒ็ฎกๅฅ—็ต„ไปถ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

2d79642e0f749d4dfbb80aa2f221e8cd

DHAS9402282805

Company Information

Product Details

Limited to the first level identification range of the "X-ray tube sleeve assembly for diagnosis (P.1760)" of the Measures for the Classification and Grading Management of Medical Equipment.

P Radiology Science

P.1760 ่จบๆ–ท็”จXๅ…‰็ƒ็ฎกๅฅ—็ต„ไปถ

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

Dates and Status

Jun 09, 2022

Jun 09, 2027

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