Primary Device ID | 00884838112742 |
NIH Device Record Key | 0ef1fdde-150f-455a-95d8-a29321ae906d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MR-RT |
Version Model Number | RTgo 5 |
Catalog Number | 781439 |
Company DUNS | 413819707 |
Company Name | Philips Medical Systems Nederland B.V. |
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 | false |
Manufacturing Date | false |
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 | 00884838112742 [Primary] |
MUJ | System, Planning, Radiation Therapy Treatment |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-09-09 |
Device Publish Date | 2022-09-01 |
00884838112780 | MR-RT is an add-on to the existing Ingenia 1.5T and 3.0T MR systems that makes the system suitab |
00884838112759 | MR-RT is an add-on to the existing Ingenia 1.5T and 3.0T MR systems that makes the system suitab |
00884838112742 | MR-RT is an add-on to the existing Ingenia 1.5T and 3.0T MR systems that makes the system suitab |
00884838122123 | MR-RT is an add-on to the existing Ingenia 1.5T and 3.0T MR systems that makes the system suitab |