Primary Device ID | 05056190500733 |
NIH Device Record Key | b5292794-509a-47be-9557-548ab63f1da4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Respiratory Module |
Version Model Number | Respiratory Module |
Catalog Number | Respiratory Module |
Company DUNS | 222160801 |
Company Name | VISION RT LIMITED |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05056190500733 [Primary] |
IYE | Accelerator, Linear, Medical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-06-24 |
Device Publish Date | 2024-06-14 |
05056190500962 - AlignRT Plus | 2024-07-31 |
05056190500979 - AlignRT Plus | 2024-07-31 |
05056190500986 - AlignRT Plus | 2024-07-31 |
05056190500733 - Respiratory Module | 2024-06-24Respiratory Module software module. |
05056190500733 - Respiratory Module | 2024-06-24 Respiratory Module software module. |
05056190500726 - AlignRT 7.3 (software) | 2024-04-11 AlignRT 7.3 (software) used on AlignRT Plus systems |
05056190500740 - DoseRT camera | 2024-04-11 DoseRT camera used for AlignRT Plus systems. |
05056190500825 - Patient ID Module | 2024-04-11 Patient ID Module used as accessory to AlignRT Plus |
05056190500894 - DoseRT reference board | 2024-04-11 DoseRT reference board used with AlignRT Plus systems. |