Taiwan FDA registration 33759e225d7acb118b6b1d5305c46b1b
Terason Ultrasound System
TW: 泰聖超音波系統
Taiwan·Risk Class 2·MD·QISDA CORPORATION·Registered Dec 02, 2013 – Dec 02, 2018CancelledRegistration details
- Analysis ID
- 33759e225d7acb118b6b1d5305c46b1b
- License Form
- Ministry of Health Medical Device Manufacturing No. 004297
Company information
- Manufacturer
- QISDA CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- QISDA CORPORATION
Product details
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P1550 ultrasonic pulsating Doppler imaging system
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Dec 02, 2013
- Expiry Date
- Dec 02, 2018
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證逾有效期未申請展延
About this record
Access comprehensive regulatory information for Terason 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 33759e225d7acb118b6b1d5305c46b1b and manufactured by QISDA CORPORATION. The authorized representative in Taiwan is QISDA CORPORATION.
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