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"Fujino" electronic endoscope - Taiwan Registration 997bcf4f26d27c287a4a6e5f1ad7c82f

Access comprehensive regulatory information for "Fujino" electronic endoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 997bcf4f26d27c287a4a6e5f1ad7c82f and manufactured by FUJIFILM Healthcare Manufacturing Corporation Hitachiomiya Office;; FUJIFILM CORPORATION. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including FUJIFILM Healthcare Manufacturing Corporation Hitachiomiya Office;; FUJIFILM CORPORATION, FUJINON MITO CORPORATION;; 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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997bcf4f26d27c287a4a6e5f1ad7c82f
Registration Details
Taiwan FDA Registration: 997bcf4f26d27c287a4a6e5f1ad7c82f
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Device Details

"Fujino" electronic endoscope
TW: "ๅฏŒๅฃซ่ƒฝ" ้›ปๅญๅผๅ…ง่ฆ–้ก
Risk Class 2

Registration Details

997bcf4f26d27c287a4a6e5f1ad7c82f

DHA00601293801

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 08, 2005

Nov 08, 2025