Taiwan FDA registration b51be4bf6385359722cc57d9d11c144f
“OMRON” Non-invasive Vascular Screening Device
TW: “歐姆龍”非侵入性血管檢測儀
Taiwan·Risk Class 2·MD·OMRON HEALTHCARE CO., LTD. MATSUSAKA FACTORY·Registered Jun 14, 2019 – Jun 14, 2024ExpiredRegistration details
- Analysis ID
- b51be4bf6385359722cc57d9d11c144f
- License Form
- Ministry of Health Medical Device Import No. 032635
- Customs Code
- DHA05603263501
Company information
- Manufacturer
- OMRON HEALTHCARE CO., LTD. MATSUSAKA FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- OMRON HEALTHCARE TAIWAN CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1130 Non-invasive blood pressure measurement system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 14, 2019
- Expiry Date
- Jun 14, 2024
About this record
Access comprehensive regulatory information for “OMRON” Non-invasive Vascular Screening Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b51be4bf6385359722cc57d9d11c144f and manufactured by OMRON HEALTHCARE CO., LTD. MATSUSAKA FACTORY. The authorized representative in Taiwan is OMRON HEALTHCARE TAIWAN CO., LTD..
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 DatabasePowered by Pure Global AI89,000+ Devices