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"Fujifilm" mobile digital X-ray system - Taiwan Registration 5a7e38384dcac9d70babed30d2c8c5f8

Access comprehensive regulatory information for "Fujifilm" mobile 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 5a7e38384dcac9d70babed30d2c8c5f8 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office;; FUJIFILM CORPORATION. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN 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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5a7e38384dcac9d70babed30d2c8c5f8
Registration Details
Taiwan FDA Registration: 5a7e38384dcac9d70babed30d2c8c5f8
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Device Details

"Fujifilm" mobile digital X-ray system
TW: โ€œๅฏŒๅฃซโ€ ็งปๅ‹•ๅผๆ•ธไฝXๅ…‰้€่ฆ–็ณป็ตฑ
Risk Class 2

Registration Details

5a7e38384dcac9d70babed30d2c8c5f8

DHAS5603655900

Product Details

Details are as detailed as approved Chinese instructions

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

Jul 01, 2023

Jul 01, 2028