Primary Device ID | 05404028000700 |
NIH Device Record Key | 85c8a946-0ba8-454f-8e9d-aaf6f1e6490a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 3-matic |
Version Model Number | 3-matic Medical |
Catalog Number | 3-matic Medical |
Company DUNS | 373139427 |
Company Name | Materialise NV |
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 | 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 | 05404028000700 [Primary] |
LLZ | System, Image Processing, Radiological |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-12-11 |
Device Publish Date | 2024-12-03 |
E3143MATICMEDICAL0 | 3-matic Medical |
E31433MATICMEDICAL0 | 3-matic Medical |
05404028000700 | 3-matic Medical |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
3-MATIC 78180356 3488585 Live/Registered |
MATERIALISE, naamloze vennootschap 2002-10-31 |