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"Fujino" electronic endoscope - Taiwan Registration 66e245785061b4208806f0d6e60bc61f

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 66e245785061b4208806f0d6e60bc61f and manufactured by FUJINON MITO CORPORATION;; FUJIFILM CORPORATION. The authorized representative in Taiwan is WELMORE CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FUJIFILM Healthcare Manufacturing Corporation Hitachiomiya 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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66e245785061b4208806f0d6e60bc61f
Registration Details
Taiwan FDA Registration: 66e245785061b4208806f0d6e60bc61f
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Device Details

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

Registration Details

66e245785061b4208806f0d6e60bc61f

DHA00601689602

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

Jul 21, 2006

Jul 21, 2021

Aug 15, 2023

Cancellation Information

Logged out

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