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"Fujifilm" electronic duodenoscopy and accessories - Taiwan Registration 617852d320eecf3d2fc7f8b5745514fc

Access comprehensive regulatory information for "Fujifilm" electronic duodenoscopy 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 617852d320eecf3d2fc7f8b5745514fc and manufactured by FUJIFILM Healthcare Manufacturing Corporation Sano 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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617852d320eecf3d2fc7f8b5745514fc
Registration Details
Taiwan FDA Registration: 617852d320eecf3d2fc7f8b5745514fc
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Device Details

"Fujifilm" electronic duodenoscopy and accessories
TW: โ€œๅฏŒๅฃซโ€้›ปๅญๅผๅไบŒๆŒ‡่…ธ้กๅŠ้™„ไปถ
Risk Class 2

Registration Details

617852d320eecf3d2fc7f8b5745514fc

DHA05603271002

Product Details

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

H Gastroenterology and urology

H.1500 Internal Scope and its accessories

import

Dates and Status

Jun 28, 2019

Jun 28, 2029