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"Fujifilm" endoscope host - Taiwan Registration e6bc50f0c87d714f6e08f424a7f639fa

Access comprehensive regulatory information for "Fujifilm" endoscope host in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e6bc50f0c87d714f6e08f424a7f639fa 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 Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION, and 2 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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e6bc50f0c87d714f6e08f424a7f639fa
Registration Details
Taiwan FDA Registration: e6bc50f0c87d714f6e08f424a7f639fa
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Device Details

"Fujifilm" endoscope host
TW: โ€œๅฏŒๅฃซโ€ๅ…ง่ฆ–้กไธปๆฉŸ
Risk Class 2

Registration Details

e6bc50f0c87d714f6e08f424a7f639fa

DHA05603401708

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

Nov 06, 2020

Nov 06, 2025

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