Taiwan FDA registration 7b239a4554e81d3f69b6f9bda0263124

Flushing equipment and accessories for Fujifilm endoscopes

TW: “富士”內視鏡用沖水設備及附件
Taiwan flagTaiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office;; FUJIFILM CORPORATION·Registered Jan 07, 2015 – Jan 07, 2030Active
Registration details
Analysis ID
7b239a4554e81d3f69b6f9bda0263124
Customs Code
DHA05602690400
Company information
Manufacturer Country
Japan
Authorized Representative
FUJIFILM HEALTHCARE TAIWAN CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
H Gastroenterology and urology
Product Type (Level 2)
H.1500 Internal Scope and its accessories
Import Information
import
Dates and status
Registration Date
Jan 07, 2015
Expiry Date
Jan 07, 2030
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About this record

Access comprehensive regulatory information for Flushing equipment and accessories for Fujifilm endoscopes in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7b239a4554e81d3f69b6f9bda0263124 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Hanamaki 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 Hanamaki Office;; FUJIFILM CORPORATION, and 1 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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