ScanPoint®
by Verathon Inc
ScanPoint® is a Class II device made by Verathon Inc, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00879123006127), registry data as of 8 Nov 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00879123006127 | Date24 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 00879123006127
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Ultrasound imaging system application software
- Model / reference
- ScanPoint®
- Primary DI / UDI-DI
- 00879123006127
- FDA product code
- IYO
- GMDN term
- Ultrasound imaging system application software
- Device class
- Class II
- Regulation number
- 892.1560
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Ultrasound imaging system application software.