Primary Device ID | 05060608880034 |
NIH Device Record Key | d668ffdc-adcf-47e7-8c64-e804f40a0931 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Daily QA 3 |
Version Model Number | 1093300Z |
Catalog Number | 1093000-0Z |
Company DUNS | 122240021 |
Company Name | SUN NUCLEAR CORP. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Special Storage Condition, Specify | Between 0 and 0 *Store the instrument in an indoor, protected environment where the instrument will not be irradiated by the direct beam |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05060608880034 [Primary] |
LHO | Instrument, Quality-Assurance, Radiologic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-10-09 |
Device Publish Date | 2019-10-01 |
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05060608881178 - Precision Cut EBT3 GafChromic™ Film | 2024-01-10 Precision Cut EBT3 GafChromic™ Film |
05060608881123 - SunSCAN 3D | 2023-06-16 The SunSCAN 3D, model 1234/1235, is intended for radiotherapy dosimetry measurements and export of those measurements for commis |
05060608881130 - SunSCAN 3D | 2023-06-16 The SunSCAN 3D, model 1234/1235, is intended for radiotherapy dosimetry measurements and export of those measurements for commis |
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05060608880102 - StereoPHAN | 2020-07-31 Radiation therapy, machine QA device |
05060608880751 - IC PROFILER | 2020-07-31 Radiation therapy QA device. |