Taiwan FDA registration f3e7f08950fd9e7d1412d437fdaf802c
“ASUS” Handheld Ultrasound Imaging System
TW: “華碩” 手持超音波影像系統
Taiwan·Risk Class 2·MD·ACME PORTABLE CORP.·Registered May 07, 2023 – May 07, 2028ActiveRegistration details
- Analysis ID
- f3e7f08950fd9e7d1412d437fdaf802c
- License Form
- Ministry of Health Medical Device Manufacturing No. 007849
Company information
- Manufacturer
- ACME PORTABLE CORP.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- ASUSTEK COMPUTER INCORPORATION
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P1550 ultrasonic pulsating Doppler imaging system
- Import Information
- Produced in Taiwan, China; Contract manufacturing
Dates and status
- Registration Date
- May 07, 2023
- Expiry Date
- May 07, 2028
About this record
Access comprehensive regulatory information for “ASUS” Handheld Ultrasound Imaging System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f3e7f08950fd9e7d1412d437fdaf802c and manufactured by ACME PORTABLE CORP.. The authorized representative in Taiwan is ASUSTEK COMPUTER INCORPORATION.
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