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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 5 of 6| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Sun Nuclear MICRO | MLB 200 | FDA UDI | Class I | Active |
| ArcCHECK PMMA MultiPlug | 12200003Z | FDA UDI | Class I | Active |
| SNC125c (BNC) | 1041600Z | EUDAMEDFDA UDI | Class II | Active |
| QED Detector, 1-4MV (-) 3m | 11140002Z | FDA UDI | Class II | Active |
| QED Detector, 15-25MV (-) 1.5m | 11160006Z | FDA UDI | Class II | Active |
| Sun Nuclear MICRO+ | MLG+350 | FDA UDI | Class I | Active |
| RapidCheck | RC1000 | FDA UDI | Class I | Active |
| SNC Phantom (kV-QA) | 1250300 | EUDAMEDFDA UDI | Class I | Active |
| SNC600c (TNC) | 10470001Z | FDA UDI | Class II | Active |
| SRS MapCHECK | 11790000Z | FDA UDI | Class II | Active |
| Sun Nuclear 115H Half Value Layer Attenuator Set | 115H | FDA UDI | Class I | Active |
| QED Detector, Skin (-) 3m | 11130002Z | FDA UDI | Class II | Active |
| ArcCHECK PMMA MultiPlug | 1220000-3Z | FDA UDI | Class I | Active |
| SNC Phantom (WL-QA) | 1253300 | FDA UDI | Class I | Active |
| Sun Nuclear MICRO+ | MLG+300 | FDA UDI | Class I | Active |
| Daily QA-MR | 1096300Z | FDA UDI | Class I | Active |
| Sun Nuclear MICRO+ MR | MLB+300MR | FDA UDI | Class I | Active |
| SNC Phantom (FS-QA) | 1252300 | EUDAMEDFDA UDI | Class I | Active |
| PC Electrometer (TNC) | 1014400Z | FDA UDI | Class II | Active |
| 6-12MV QED Detector (3m Cable) | 11150003Z | FDA UDI | Class II | Unknown |
| CT Sim+ | CT Sim+ | FDA UDI | Class I | Active |
| Mapcheck2, Arccheck | K131466 | FDA 510(k) | Class II | Active |
| Cal/Rad Upgrade Model 1030 | K880272 | FDA 510(k) | Class II | Active |
| Profiler 2 | K063021 | FDA 510(k) | Class II | Active |
| Sun 125c Ionization Chamber | K112981 | FDA 510(k) | Class II | Active |
| Rf-Ivd Wireless Dosimeter-Model 1133 | K011332 | FDA 510(k) | Class II | Active |
| Qed Diode Detectors, Models 1112-1116 | K011466 | FDA 510(k) | Class II | Active |
| Perfraction | K141800 | FDA 510(k) | Class II | Active |
| Quality Reports | K142142 | FDA 510(k) | Class II | Active |
| Dose Calculator | K150848 | FDA 510(k) | Class II | Active |
| 3dvh | K131862 | FDA 510(k) | Class II | Active |
| Re-Entrant Chamber | K013689 | FDA 510(k) | Class II | Active |
| Model 1014 Pc Electrometer | K092019 | FDA 510(k) | Class II | Active |
| Epidose | K131704 | FDA 510(k) | Class II | Active |
| Ivd (in Vivo Dosimeter), Model 1131 | K010449 | FDA 510(k) | Class II | Active |
| Model 1133 Ivd Pc Version | K021463 | FDA 510(k) | Class II | Active |
| ArcCHECK-MR | K160057 | EUDAMEDFDA 510(k)FDA UDI | Class II | Active |
| DoseCHECK | K161946 | FDA 510(k) | Class II | Active |
| WaterProof PROFILER | K142431 | FDA 510(k)FDA UDI | Class II | Active |
| Re-Entrant Chamber, Model 1008 Or 44d | K002446 | FDA 510(k) | Class II | Active |
| 3d Scanner, Model 1230 | K101992 | FDA 510(k) | Class II | Active |
| The Edge Detector, Model 1118 | K051921 | FDA 510(k) | Class II | Active |
| Precision Dosimetry Electrometer, Model 1010 Or 206 | K002444 | FDA 510(k) | Class II | Active |
| StereoPHAN | 1255 | EUDAMED | Class I | Active |
| ArcCHECK | 1220 | EUDAMEDFDA UDI | Class IIb | Active |
| SunCHECK | 1299 | EUDAMEDFDA UDI | Class IIb | Active |
| Daily QA 3 | 1093 | EUDAMEDFDA UDI | Class IIb | Active |
| SunSILICON | 1048 | EUDAMEDFDA UDI | Class IIb | Active |
| Daily QA 4 Pro | 1098 | EUDAMED | Class IIb | Active |
| SunSILICON P | 1049 | EUDAMEDFDA UDI | Class IIb | Active |
Related Companies
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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. |