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"Kodak" digital X-ray system - Taiwan Registration 5c4a7e7d0b2a1957ede4207ff5772bbf

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 5c4a7e7d0b2a1957ede4207ff5772bbf and manufactured by RAYCO (SHANGHAI) MEDICAL PRODUCTS COMPANY LIMITED. 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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5c4a7e7d0b2a1957ede4207ff5772bbf
Registration Details
Taiwan FDA Registration: 5c4a7e7d0b2a1957ede4207ff5772bbf
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Device Details

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

Registration Details

5c4a7e7d0b2a1957ede4207ff5772bbf

DHAS4200014600

Company Information

Product Details

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

P Radiology Science

P.1680 ๅ›บๅฎšๅผXๅ…‰็ณป็ตฑ

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

Dates and Status

Nov 13, 2006

Nov 13, 2011

Jan 17, 2013

Cancellation Information

Logged out

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