EOSedge 3
by Eos Imaging
EOSedge 3 (EOSEDGE30NA) is a Class II device made by Eos Imaging, listed in FDA GUDID since 14 May 2025 (UDI-DI 03663999000405), registry data as of 12 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 | Number03663999000405 | Date14 May 2025 | StatusListed |
Official records
- AccessGUDID record 03663999000405
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- EOSedge
- Generic name
- Stationary basic diagnostic x-ray system, digital
- Model / Ref / Catalog
- 3, EOSEDGE30NA
- Primary DI / UDI-DI
- 03663999000405
- FDA product code
- KPR
- GMDN term
- Stationary basic diagnostic x-ray system, digital
- Device class
- Class II
- Regulation number
- 892.1680
- GUDID distribution status
- In Commercial Distribution
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