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"Fujifilm film" general photographic X-ray device - Taiwan Registration d79d88e4ec245e2c5d44709a0798c370

Access comprehensive regulatory information for "Fujifilm film" general photographic X-ray device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d79d88e4ec245e2c5d44709a0798c370 and manufactured by FUJIFILM Healthcare Corporation Medical System Operations Group, Kashiwa. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FUJIFILM Healthcare Corporation Medical System Operations Group, Kashiwa, 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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d79d88e4ec245e2c5d44709a0798c370
Registration Details
Taiwan FDA Registration: d79d88e4ec245e2c5d44709a0798c370
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Device Details

"Fujifilm film" general photographic X-ray device
TW: โ€œๅฏŒๅฃซ่ปŸ็‰‡โ€ไธ€่ˆฌๆ”ๅฝฑXๅ…‰่ฃ็ฝฎ
Risk Class 2

Registration Details

d79d88e4ec245e2c5d44709a0798c370

DHAS5603357404

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

Apr 28, 2020

Apr 28, 2025

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