Taiwan FDA registration b0c2fc1514f25ec6e47c2966685a29f1
“TERATECH” uSmart3200T Ultrasound System Transducers
TW: “特諾克”超音波探頭
Taiwan·Risk Class 2·MD·TERATECH CORPORATION·Registered Dec 02, 2013 – Dec 02, 2018CancelledRegistration details
- Analysis ID
- b0c2fc1514f25ec6e47c2966685a29f1
- License Form
- Ministry of Health Medical Device Import No. 025647
- Customs Code
- DHA05602564701
Company information
- Manufacturer
- TERATECH CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- QISDA CORPORATION
Product details
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P1570 Ultrasound converter for diagnostics
- Import Information
- Imported from abroad
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 “TERATECH” uSmart3200T Ultrasound System Transducers in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b0c2fc1514f25ec6e47c2966685a29f1 and manufactured by TERATECH CORPORATION. The authorized representative in Taiwan is QISDA CORPORATION.
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