Identity
- Trade Name
- SNC Phantom (WL-QA) FDA UDI
- Generic Name
- Accelerator system quality assurance device FDA UDI
- Device Name
- Radiation therapy, machine QA device FDA UDI
- Model / Reference
- 1253300 FDA UDI
- Description
- Radiation therapy, machine QA device FDA UDI
Identifiers
- Catalog Number
- 1253300 FDA UDI
- Primary DI / UDI-DI
- 05060608880966 FDA UDI
- FDA Product Code
- IXG FDA UDI
- GMDN Term
- Accelerator system quality assurance device FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 892.1950 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Accelerator system quality assurance device
SNC Phantom (WL-QA) by Sun Nuclear Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Accelerator system quality assurance device.
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- Detector Holder — IBA Dosimetry GmbH · Class II
- myQA®Daily (Software) — IBA Dosimetry GmbH · Class I
- Vista — Modus Medical Devices Inc · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Sun Nuclear Corporation
Sources (1)
- FDA UDI 57af5c90-265e-4bdf-86ff-976e08bb05bc 35 fields · synced Jun 8, 2026