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"Ayindi" mobile X-ray system - Taiwan Registration b2045cc00f3984e7d2c35cb0697c8049

Access comprehensive regulatory information for "Ayindi" mobile 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 b2045cc00f3984e7d2c35cb0697c8049 and manufactured by INTERMEDICAL S.R.L.. The authorized representative in Taiwan is FONN CHANG TRADING CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including I.M.D. INTERNATIONAL MEDICAL DEVICES S.P.A., 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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b2045cc00f3984e7d2c35cb0697c8049
Registration Details
Taiwan FDA Registration: b2045cc00f3984e7d2c35cb0697c8049
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Device Details

"Ayindi" mobile X-ray system
TW: โ€œ่‰พๅฝฅ่ฟชโ€็งปๅ‹•ๅผXๅ…‰็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

b2045cc00f3984e7d2c35cb0697c8049

DHAS0602290204

Company Information

Italy

Product Details

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

P Radiology Science

P.1720 ็งปๅ‹•ๅผXๅ…‰็ณป็ตฑ

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

Oct 24, 2011

Oct 24, 2016

Aug 21, 2018

Cancellation Information

Logged out

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