“HITACHI” Digital Diagnostic Ultrasound Scanner
Taiwan·Risk Class 2·MD·Hitachi Healthcare Manufacturing, Ltd. Analytical Systems Kashiwa Factory·Registered Aug 19, 2014 – Aug 19, 2024Expired- Analysis ID
- e4bbfa096cf6f0cbd6786a7ba15d8117
- License Form
- Ministry of Health Medical Device Import No. 026440
- Customs Code
- DHA05602644000
- Manufacturer Country
- Japan
- Authorized Representative
- Taiwan Health Fujifilm Medical Equipment Co., Ltd
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P1550 ultrasonic pulsating Doppler imaging system
- Import Information
- Imported from abroad
- Registration Date
- Aug 19, 2014
- Expiry Date
- Aug 19, 2024
- Cancellation Date
- Mar 08, 2023
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Access comprehensive regulatory information for “HITACHI” Digital Diagnostic Ultrasound Scanner in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e4bbfa096cf6f0cbd6786a7ba15d8117 and manufactured by Hitachi Healthcare Manufacturing, Ltd. Analytical Systems Kashiwa Factory. The authorized representative in Taiwan is Taiwan Health Fujifilm Medical Equipment Co., Ltd.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Hitachi, Ltd. Medical System Operations Group, Kashiwa, 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.