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"Kodak" full-port digital X-ray system - Taiwan Registration 66d9f2e9d2a80ebfc054fd7933535df5

Access comprehensive regulatory information for "Kodak" full-port 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 66d9f2e9d2a80ebfc054fd7933535df5 and manufactured by TROPHY. The authorized representative in Taiwan is Taiwan Kangshi Medical Equipment Co., Ltd.

This page provides complete technical specifications, regulatory compliance details. 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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66d9f2e9d2a80ebfc054fd7933535df5
Registration Details
Taiwan FDA Registration: 66d9f2e9d2a80ebfc054fd7933535df5
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Device Details

"Kodak" full-port digital X-ray system
TW: โ€œๆŸฏ้”โ€ๅ…จๅฃๆ•ธไฝXๅ…‰็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

66d9f2e9d2a80ebfc054fd7933535df5

DHAS0601977207

Company Information

France

Product Details

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

F Dentistry

F.1800 ๅฃ่…”ๅค–Xๅ…‰็…งๅฐ„็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

Apr 09, 2009

Apr 09, 2014

Jan 09, 2017

Cancellation Information

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