"Fujifilm" endoscopic ultrasound host
Taiwan·Risk Class 2·FUJIFILM TECHNO PRODUCTS CO., LTD. TOHOKU FACTORY HANAMAKI SITE·Registered Jun 05, 2012 – Jun 05, 2022Cancelled- Analysis ID
- cae5a442c830b43c8ff89c77f9ca7911
- Customs Code
- DHA00602352602
- Manufacturer Country
- Japan
- Authorized Representative
- FUJIFILM HEALTHCARE TAIWAN CO., LTD.
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1550 Ultrasonic pulsating Duppler imaging system
- Import Information
- import
- Registration Date
- Jun 05, 2012
- Expiry Date
- Jun 05, 2022
- Cancellation Date
- Apr 12, 2024
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for "Fujifilm" endoscopic ultrasound host in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cae5a442c830b43c8ff89c77f9ca7911 and manufactured by FUJIFILM TECHNO PRODUCTS CO., LTD. TOHOKU FACTORY HANAMAKI SITE. 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 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.