Pure Global

Fujifilm Digital Photography System - Taiwan Registration cdd7048852e8e9cc64827c397014292b

Access comprehensive regulatory information for Fujifilm Digital Photography System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cdd7048852e8e9cc64827c397014292b and manufactured by FUJIFILM TECHNO PRODUCTS CO., LTD. TOHOKU FACTORY HANAMAKI SITE. The authorized representative in Taiwan is NAN KAI CORPORATION.

This page provides complete technical specifications, regulatory compliance details. 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
cdd7048852e8e9cc64827c397014292b
Registration Details
Taiwan FDA Registration: cdd7048852e8e9cc64827c397014292b
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Fujifilm Digital Photography System
TW: ๅฏŒๅฃซๆ•ธไฝๆ”ๅฝฑ็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

cdd7048852e8e9cc64827c397014292b

DHA00602485102

Company Information

Product Details

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

P Radiology Science

P.1650 ้€่ฆ–Xๅ…‰ๅฝฑๅƒๅขžๆ„Ÿ็ฎก

import

Dates and Status

Apr 03, 2013

Apr 03, 2018

Dec 13, 2019

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ