eRAD RIS 4.22
by Erad, Inc.
eRAD RIS 4.22 is a Class I device made by Erad, Inc., listed in FDA GUDID since 6 Dec 2022 (UDI-DI 00866994000262), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00866994000262 | Date6 Dec 2022 | StatusListed |
Official records
- AccessGUDID record 00866994000262
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- eRAD RIS
- Generic name
- Radiology information system application software
- Model / reference
- 4.22
- Primary DI / UDI-DI
- 00866994000262
- FDA product code
- LMD
- GMDN term
- Radiology information system application software
- Device class
- Class I
- Regulation number
- 892.2020
- GUDID distribution status
- In Commercial Distribution
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