Taiwan FDA registration 80fa451e338e99c1d8a9684e9e9e61b1
"ASUS" ultrasound imager
TW: “華碩”超音波影像儀
Taiwan·Risk Class 2·ACME PORTABLE CORP.·Registered Jul 23, 2020 – May 07, 2025ExpiredRegistration details
- Analysis ID
- 80fa451e338e99c1d8a9684e9e9e61b1
Company information
- Manufacturer
- ACME PORTABLE CORP.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- LELTEK INC.
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
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Jul 23, 2020
- Expiry Date
- May 07, 2025
About this record
Access comprehensive regulatory information for "ASUS" ultrasound imager in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 80fa451e338e99c1d8a9684e9e9e61b1 and manufactured by ACME PORTABLE CORP.. The authorized representative in Taiwan is LELTEK INC..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices