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"Fujifilm" electronic bronchoscope - Taiwan Registration c2761da94ef24c967f73e64382a26eee

Access comprehensive regulatory information for "Fujifilm" electronic bronchoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c2761da94ef24c967f73e64382a26eee 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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c2761da94ef24c967f73e64382a26eee
Registration Details
Taiwan FDA Registration: c2761da94ef24c967f73e64382a26eee
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Device Details

"Fujifilm" electronic bronchoscope
TW: โ€œๅฏŒๅฃซโ€้›ปๅญๅผๆ”ฏๆฐฃ็ฎก้ก
Risk Class 2

Registration Details

c2761da94ef24c967f73e64382a26eee

DHA00602361001

Product Details

For details, it is Chinese approved copy of the imitation order

G ENT Science

G.4680 Bronchial tubescopes (soft or rigid) and accessories thereof

import

Dates and Status

Jun 06, 2012

Jun 06, 2027

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