Taiwan FDA registration 50e039a69809e3363a9e87bbf424605d

"Fujifilm" endoscopic ultrasound host

TW: “富士”內視鏡超音波主機
Taiwan flagTaiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION·Registered Dec 20, 2016 – Dec 20, 2026Active
Registration details
Analysis ID
50e039a69809e3363a9e87bbf424605d
Customs Code
DHA05602914701
Company information
Manufacturer Country
Japan
Authorized Representative
FUJIFILM HEALTHCARE TAIWAN CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
P Radiology Science
Product Type (Level 2)
P.1550 Ultrasonic pulsating Duppler imaging system
Import Information
import
Dates and status
Registration Date
Dec 20, 2016
Expiry Date
Dec 20, 2026
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About this record

Access comprehensive regulatory information for "Fujifilm" endoscopic ultrasound host in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 50e039a69809e3363a9e87bbf424605d 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, 1 companies making similar products including FUJIFILM TECHNO PRODUCTS CO., LTD. TOHOKU FACTORY HANAMAKI SITE, 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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