Primary Device ID | 04056481145880 |
NIH Device Record Key | 8abae08b-2dbf-4b95-bdcf-97d0b028d96e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Contouring |
Version Model Number | 5.0 |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04056481145880 [Primary] |
QIH | Automated Radiological Image Processing Software |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-07-04 |
Device Publish Date | 2025-06-26 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() CONTOURING 87861480 5557554 Live/Registered |
medi GmbH & Co. KG 2018-04-03 |