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"Kodak" digital X-ray system - Taiwan Registration 971417116800641be3d6c19c2ab2d68c

Access comprehensive regulatory information for "Kodak" digital 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 971417116800641be3d6c19c2ab2d68c and manufactured by CARESTREAM HEALTH,INC.. The authorized representative in Taiwan is Taiwan Kangshi Medical Equipment Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including CARESTREAM HEALTH,INC. EQUIPMENT DEVELOPMENT AND MANUFACTURING, RAYCO (SHANGHAI) MEDICAL PRODUCTS COMPANY LIMITED, and 3 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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971417116800641be3d6c19c2ab2d68c
Registration Details
Taiwan FDA Registration: 971417116800641be3d6c19c2ab2d68c
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Device Details

"Kodak" digital X-ray system
TW: "ๆŸฏ้”" ๆ•ธไฝXๅ…‰็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

971417116800641be3d6c19c2ab2d68c

DHAS0601373803

Company Information

United States

Product Details

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

P Radiology Science

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

Dates and Status

Dec 05, 2005

Dec 05, 2015

May 28, 2018

Cancellation Information

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