Primary Device ID | 04056481140397 |
NIH Device Record Key | 34ba5469-6149-45d7-9dc0-bc2cfdc324b8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RT QA |
Version Model Number | 1.5 |
Catalog Number | 21762-02A |
Company DUNS | 314482980 |
Company Name | Brainlab AG |
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 | true |
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 | false |
OTC Over-The-Counter | false |
Phone | +49899915680 |
contact@brainlab.com | |
Phone | +49899915680 |
contact@brainlab.com | |
Phone | +49899915680 |
contact@brainlab.com | |
Phone | +49899915680 |
contact@brainlab.com | |
Phone | +49899915680 |
contact@brainlab.com | |
Phone | +49899915680 |
contact@brainlab.com | |
Phone | +49899915680 |
contact@brainlab.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04056481140397 [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 | 2018-08-20 |
Device Publish Date | 2018-07-19 |
04056481143916 - Spine Planning | 2024-11-13 |
04056481144654 - Viewer 5.4 | 2024-11-13 |
04056481143527 - DICOM Proxy | 2024-11-01 |
04056481144913 - CRANIAL 4PI STEREOTACTIC MASK (5 PCS.) | 2024-07-26 |
04056481144920 - CRANIAL 4PI STEREOTACTIC MASK (1 PC.) | 2024-07-26 |
04056481144937 - CRANIAL 4PI BASIC MASK (5 PCS.) | 2024-07-26 |
04056481144944 - CRANIAL 4PI BASIC MASK (1 PC.) | 2024-07-26 |
04056481144951 - CRANIAL 4PI OPEN FACE MASK (5 PCS.) | 2024-07-26 |