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"Singular" fluoroscopic X-ray system - Taiwan Registration d3513a8cddfb526b0c1eae4e529bd0fc

Access comprehensive regulatory information for "Singular" fluoroscopic X-ray system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d3513a8cddfb526b0c1eae4e529bd0fc and manufactured by GE OEC MEDICAL SYSTEMS INC. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including GENERAL MEDICAL MERATE S.P.A., GE MEDICAL SYSTEMS S.A., 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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d3513a8cddfb526b0c1eae4e529bd0fc
Registration Details
Taiwan FDA Registration: d3513a8cddfb526b0c1eae4e529bd0fc
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Device Details

"Singular" fluoroscopic X-ray system
TW: "ๅฅ‡็•ฐ" ้€่ฆ–Xๅ…‰็ณป็ตฑ
Risk Class 2

Registration Details

d3513a8cddfb526b0c1eae4e529bd0fc

DHAS0601197201

Company Information

United States

Product Details

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

P Radiology Science

P.1660 ้ž้€่ฆ–Xๅ…‰ๅฝฑๅƒๅขžๆ„Ÿ็ฎก

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

Sep 20, 2005

Sep 20, 2025