DicomForward 3
by Radius
DicomForward 3 is a Class I device made by Radius, listed in FDA GUDID since 24 Aug 2019 (UDI-DI B295DICOMFWD30), 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 | NumberB295DICOMFWD30 | Date24 Aug 2019 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- DicomForward
- Generic name
- Diagnostic imaging telemedicine system
- Model / reference
- 3
- Primary DI / UDI-DI
- B295DICOMFWD30
- FDA product code
- LMD
- GMDN term
- Diagnostic imaging telemedicine system
- Device class
- Class I
- Regulation number
- 892.2020
- GUDID distribution status
- In Commercial Distribution
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