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Sign in to claim this brandSun Nuclear Corporation
United States·US-MF-000021541
Last updated September 18, 2026
About
Sun Nuclear is the source for independent, integrated solutions for Quality Management throughout the diagnosis and treatment of cancer.
From the manufacturer's own website. Source
Information
- Country
- United States
- Address
- 900, Asbury Avenue, Norfolk, United States
- Website
- www.sunnuclear.com
- [email protected]
- Phone
- +16088287000
- PRRC Contact
- Jeff Shaw
- EUDAMED SRN
- US-MF-000021541
- FDA FEI Number
- 1038814
- DUNS Number
- —
Catalogue (251)
Page 3 of 6| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| 6-12MV QED Detector (3m Cable) | 11150002Z | FDA UDI | Class II | Unknown |
| Profiler 2 | 11740000Z | FDA UDI | Class II | Unknown |
| EPIDose | 12140000 | FDA UDI | Class II | Active |
| QED Detector, 15-25MV (+) 3m | 11160003Z | FDA UDI | Class II | Active |
| 3d Tpr | 1230680Z | FDA UDI | Class II | Unknown |
| Sun Nuclear IB3 Inner Bone | 456 | FDA UDI | Class I | Active |
| EPIDose | 1214 | FDA UDI | Class II | Active |
| SRS MapCHECK | 1179300Z | FDA UDI | Class II | Active |
| Electron QED Detector (3m Cable) | 11120002Z | FDA UDI | Class II | Unknown |
| 1-4MV QED Detector (3m Cable) | 11140002Z | FDA UDI | Class II | Unknown |
| 1-4 MV ISORAD Detector (3m Cable) | 11620002Z | FDA UDI | Class II | Unknown |
| 3D SCANNER TPR Option | 12300004Z | FDA UDI | Class II | Unknown |
| Sun Nuclear MICRO | MLR 150 | FDA UDI | Class I | Active |
| rf-IVD 2 | 11360000Z | FDA UDI | Class II | Active |
| SunSCAN 3D | 1235 | EUDAMEDFDA UDI | Class II | Active |
| Sun Nuclear LN-450 Lung TMM | 485 | FDA UDI | Class I | Active |
| Skin QED Detector (1.5m Cable) | 11130006Z | FDA UDI | Class II | Unknown |
| ISORAD Detector, 6-12MV (-) 1.5m | 11630006Z | FDA UDI | Class II | Active |
| Ic Profiler | 1122800Z | EUDAMEDFDA UDI | Class I | Active |
| 3d Scanner (tnc) | 12300000TZ | FDA UDI | Class II | Active |
| 15-25MV QED Detector (3m Cable) | 11160002Z | FDA UDI | Class II | Unknown |
| Varian IMF (Isocentric Mounting Fixture) | 1177000VZ | FDA UDI | Class II | Active |
| Sun Nuclear CT Solid Water | 451 | FDA UDI | Class I | Active |
| PerFRACTION | 12150000Z | FDA UDI | Class II | Active |
| ISORAD Detector, 1-4MV (-) 3m | 11620002Z | FDA UDI | Class II | Active |
| SNC350p (BNC) | 10450000Z | FDA UDI | Class II | Active |
| 1-4MV QED Detector (3m Cable) | 11140003Z | FDA UDI | Class II | Unknown |
| 15-25 MV ISORAD Detector (3m Cable) | 11640002Z | FDA UDI | Class II | Unknown |
| 15-25MV QED Detector (3m Cable) | 11160003Z | FDA UDI | Class II | Unknown |
| rf-Daily QA 3 | 1093500Z | EUDAMEDFDA UDI | Class I | Active |
| Electron Quad Wedge Plate | 1122656Z | FDA UDI | Class I | Active |
| Sun Nuclear CB2 + 30% CaCO3 TMM | 484 | FDA UDI | Class I | Active |
| Sun Nuclear | 557 | FDA UDI | Class I | Active |
| Sun Nuclear BR12 Breast | 453 | FDA UDI | Class I | Active |
| CT Sim+ | CT Sim+ | FDA UDI | Class I | Active |
| Sun Nuclear MICRO+ MR | MLR+350MR | FDA UDI | Class I | Active |
| ArcCHECK-MR | 12200000MR | FDA UDI | Class II | Unknown |
| ISORAD Detector, 15-25MV (+) 3m | 11640003Z | FDA UDI | Class II | Active |
| Electron QED Detector (3m Cable) | 11120003Z | FDA UDI | Class II | Unknown |
| Sun Nuclear 115A Half Value Layer Attenuator Set | 115A | FDA UDI | Class I | Active |
| MapPHAN (5cm) | 10830000 | FDA UDI | Class I | Active |
| Sun Nuclear Mammo 156D Stereo Phantom | 156D | EUDAMEDFDA UDI | Class I | Active |
| Skin QED Detector (3m Cable) | 11130002Z | FDA UDI | Class II | Unknown |
| Sun Nuclear MICRO+ | MLB+350 | FDA UDI | Class I | Active |
| CT Sim | 805427 | FDA UDI | Class I | Unknown |
| 6-12 MV ISORAD Detector, (1.5m Cable) | 11630006Z | FDA UDI | Class II | Unknown |
| DoseCHECK | 12170000 | FDA UDI | Class II | Active |
| CT Sim+ | CT Sim+ | FDA UDI | Class I | Active |
| 3d Tpr | 1230000-4Z | FDA UDI | Class II | Active |
| Sun Nuclear MICRO+ | MLR+300 | FDA UDI | Class I | Active |
Related Companies
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Importers
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Authorities
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FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Aug 8, 2014 | Z-0959-2015 | — | terminated | Has a Potential Pinch Hazard to user performing Machine QA in an MRI environment. |