Taiwan FDA registration dc4e85177a62056e1f71aa2112573c7e
"Inosel" Ultrasound system for diagnostics
TW: “伊諾賽” 診斷用超音波系統
Taiwan·Risk Class 2·Jiastar Technology Co., Ltd. Double Star Factory 2·Registered Sep 15, 2017 – Sep 15, 2027ActiveRegistration details
- Analysis ID
- dc4e85177a62056e1f71aa2112573c7e
- Customs Code
- DHY05500586903
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- QISDA CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1550 Ultrasonic pulsating Duppler imaging system
- Import Information
- Medical equipment produced in bonded factories; Domestic
Dates and status
- Registration Date
- Sep 15, 2017
- Expiry Date
- Sep 15, 2027
About this record
Access comprehensive regulatory information for "Inosel" Ultrasound system for diagnostics in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dc4e85177a62056e1f71aa2112573c7e and manufactured by Jiastar Technology Co., Ltd. Double Star Factory 2. The authorized representative in Taiwan is QISDA CORPORATION.
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