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"Fujifilm" ultrasound endoscope airbag (unsterilized) - Taiwan Registration 4b68b2f51d9fb1f87f5fb284264b4c30

Access comprehensive regulatory information for "Fujifilm" ultrasound endoscope airbag (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4b68b2f51d9fb1f87f5fb284264b4c30 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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4b68b2f51d9fb1f87f5fb284264b4c30
Registration Details
Taiwan FDA Registration: 4b68b2f51d9fb1f87f5fb284264b4c30
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Device Details

"Fujifilm" ultrasound endoscope airbag (unsterilized)
TW: โ€œๅฏŒๅฃซโ€่ถ…้Ÿณๆณขๅ…ง่ฆ–้ก็”จๆฐฃๅ›Š(ๆœชๆป…่Œ)
Risk Class 2

Registration Details

4b68b2f51d9fb1f87f5fb284264b4c30

DHA05603109309

Company Information

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

May 23, 2018

May 23, 2028