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"Fujifilm" mobile digital X-ray photography system and accessories - Taiwan Registration aeca4ec33dae512904be5c1d02fba1cf

Access comprehensive regulatory information for "Fujifilm" mobile digital X-ray photography system and accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number aeca4ec33dae512904be5c1d02fba1cf and manufactured by FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office;; FUJIFILM CORPORATION. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..

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aeca4ec33dae512904be5c1d02fba1cf
Registration Details
Taiwan FDA Registration: aeca4ec33dae512904be5c1d02fba1cf
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Device Details

"Fujifilm" mobile digital X-ray photography system and accessories
TW: โ€œๅฏŒๅฃซโ€็งปๅ‹•ๅผๆ•ธไฝXๅ…‰ๆ”ๅฝฑ็ณป็ตฑๅŠ้…ไปถ
Risk Class 2

Registration Details

aeca4ec33dae512904be5c1d02fba1cf

DHAS5603266502

Product Details

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

P Radiology Science

P.1720 ็งปๅ‹•ๅผ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

Jul 16, 2019

Jul 16, 2029