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"Singular" fluoroscopic X-ray system - Taiwan Registration 68af0d634fd08ade0e04080894fd77ed

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 68af0d634fd08ade0e04080894fd77ed and manufactured by GE MEDICAL SYSTEMS S.A.. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..

This page provides complete technical specifications, regulatory compliance details, 4 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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68af0d634fd08ade0e04080894fd77ed
Registration Details
Taiwan FDA Registration: 68af0d634fd08ade0e04080894fd77ed
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Device Details

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

Registration Details

68af0d634fd08ade0e04080894fd77ed

DHAS0601260202

Company Information

France

Product Details

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

P Radiology Science

P.1650 ้€่ฆ–Xๅ…‰ๅฝฑๅƒๅขžๆ„Ÿ็ฎก

Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)

Dates and Status

Oct 04, 2005

Oct 04, 2015

Apr 25, 2018

Cancellation Information

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