Fuji Systems Corporation, Shirakawa Plant
TaiwanJapan9 products registeredJul 10, 2006 – Apr 20, 2020
VerifiedTFDA · Taiwan Food and Drug Administration registry
9
Total products
9
Product types
7
Active products
Apr 2020
Latest registration
Company details
- Address
- 200-2 Aza-Ohira, Odakura, Nishigo Nishi Shirakawa Gun, Fukushima 961-8061, Japan
Regulatory footprint
Search Fuji Systems Corporation, Shirakawa Plant across other regulatory registries
Recent registrations
Latest 5 products registered by this manufacturer
“Fuji” AP-GRIPFLOW Circulation Perfusion Catheter
Class 2
Apr 20, 2020
"Fuji" circulating irrigation conduit
Class 2
Apr 06, 2020
"Fujifilm Systems" instrument and equipment protective sleeve (sterilization)
Class 1
Oct 07, 2019
“Medtronic” CELLO balloon guide catheter
Class 2
May 02, 2016
"FUJI" TREX Nonresorbable gauze/sponge for external use (Non-Sterile)
Class 1
Aug 14, 2015
Most popular products
Products with most registrations
“Fuji” AP-GRIPFLOW Circulation Perfusion Catheter
1 registrations
"Fuji" circulating irrigation conduit
1 registrations
"Fujifilm Systems" instrument and equipment protective sleeve (sterilization)
1 registrations
“Medtronic” CELLO balloon guide catheter
1 registrations
"FUJI" TREX Nonresorbable gauze/sponge for external use (Non-Sterile)
1 registrations
Authorized representatives
Taiwan authorized representatives for this manufacturer
Recent registered products
Most recent products (showing top 20)
“Fuji” AP-GRIPFLOW Circulation Perfusion Catheter
Registered: Apr 20, 2020 • Expires: Apr 20, 2025
- Risk Class
- Class 2
- Type
- MD
- AR
- YOO-HOO Limited
"Fuji" circulating irrigation conduit
Registered: Apr 06, 2020 • Expires: Apr 06, 2030
- Risk Class
- Class 2
- AR
- YOO-HOO Limited
"Fujifilm Systems" instrument and equipment protective sleeve (sterilization)
Registered: Oct 07, 2019 • Expires: Oct 07, 2029
- Risk Class
- Class 1
- AR
- Meide Medical Devices Co., Ltd
“Medtronic” CELLO balloon guide catheter
Registered: May 02, 2016 • Expires: May 02, 2026
- Risk Class
- Class 2
- Type
- MD
- AR
- MEDTRONIC (TAIWAN) LTD.
"FUJI" TREX Nonresorbable gauze/sponge for external use (Non-Sterile)
Registered: Aug 14, 2015 • Expires: Aug 14, 2020
Cancelled
- Risk Class
- Class 1
- Type
- MD
- AR
- BIOTRONIC INSTRUMENT ENTERPRISE LTD.
"Fushi" bronchial tube blocker
Registered: Feb 25, 2013 • Expires: Feb 25, 2028
- Risk Class
- Class 2
- AR
- BIOTRONIC INSTRUMENT ENTERPRISE LTD.
"Fusch" bronchial atresia catheter
Registered: Feb 21, 2013 • Expires: Feb 21, 2023
- Risk Class
- Class 2
- AR
- BIOTRONIC INSTRUMENT ENTERPRISE LTD.
"Fuji" Serbronchial atresia catheter
Registered: Jan 09, 2013 • Expires: Jan 09, 2018
Cancelled
- Risk Class
- Class 2
- AR
- BIOTRONIC INSTRUMENT ENTERPRISE LTD.
"Fujifilm" silicone self-catheter
Registered: Jul 10, 2006 • Expires: Jul 10, 2026
- Risk Class
- Class 2
- AR
- MING HWAY TRADING CO., LTD.
About this profile
Explore comprehensive manufacturer profile for Fuji Systems Corporation, Shirakawa Plant based in Japan through Pure Global AI's free Taiwan medical device database. This manufacturer has 9 products registered in Taiwan across 9 unique product categories. Their regulatory history spans from Jul 10, 2006 to Apr 20, 2020.
This page provides detailed insights including 5 recent product registrations, 5 most popular products with “Fuji” AP-GRIPFLOW Circulation Perfusion Catheter having 1 registrations, and 3 authorized representatives including BIOTRONIC INSTRUMENT ENTERPRISE LTD.. Pure Global AI offers free access to Taiwan's medical device database, enabling global MedTech companies to analyze market dynamics and identify opportunities.