Primary Device ID | 05404028000571 |
NIH Device Record Key | 2f418f25-a999-4934-b823-081296015d4c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Mimics Cardiac Planner |
Version Model Number | Mimics Cardiac Planner |
Catalog Number | Mimics Cardiac Planner |
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 | 05404028000571 [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 | 2024-03-25 |
Device Publish Date | 2024-03-15 |
05404028000571 - Mimics Cardiac Planner | 2024-03-25Mimics Cardiac Planner |
05404028000571 - Mimics Cardiac Planner | 2024-03-25 Mimics Cardiac Planner |
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