Taiwan FDA registration 8da55a0eca29c814d0bb2631a11ea82c
"Canon" Aplio i900/i800/i700 Diagnostic Ultrasound System
TW: "佳能"診斷超音波系統
Taiwan·Risk Class 2·MD·Canon Medical Systems Corporation·Registered Mar 29, 2018 – Mar 29, 2028ActiveRegistration details
- Analysis ID
- 8da55a0eca29c814d0bb2631a11ea82c
- License Form
- Ministry of Health Medical Device Import No. 030790
- Customs Code
- DHA05603079000
Company information
- Manufacturer
- Canon Medical Systems Corporation
- Manufacturer Country
- Japan
- Authorized Representative
- ROTARY TRADING CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P1550 ultrasonic pulsating Doppler imaging system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 29, 2018
- Expiry Date
- Mar 29, 2028
About this record
Access comprehensive regulatory information for "Canon" Aplio i900/i800/i700 Diagnostic Ultrasound System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8da55a0eca29c814d0bb2631a11ea82c and manufactured by Canon Medical Systems Corporation. The authorized representative in Taiwan is ROTARY TRADING CO., LTD..
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