Primary Device ID | 00840682102780 |
NIH Device Record Key | 7d0f5981-c334-42b4-8692-e5968f6cb5d5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 4D View |
Version Model Number | 16 |
Company DUNS | 300599979 |
Company Name | GE Healthcare Austria GmbH & Co OG |
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 |