Primary Device ID | 00195278517340 |
NIH Device Record Key | 655c5258-5003-4eb6-ac2e-9d73a64fc21c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ViewPoint |
Version Model Number | 6. ver14 |
Catalog Number | H47591YA |
Company DUNS | 507406770 |
Company Name | GE Healthcare GmbH |
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 | 00195278517340 [Primary] |
LLZ | System, image processing, radiological |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2023-10-18 |
Device Publish Date | 2023-02-15 |
00840682145718 | 6. ver11 |
00840682140744 | 6. ver10 |
00840682124454 | 6. ver6.9 |
00840682119627 | 6 ver6.8 |
00840682119610 | ver5.6 |
00840682103640 | 6 ver 6.7 |
00840682171953 | 6. ver12 |
00195278517340 | ViewPoint 6 v6.14 |
00195278753472 | ViewPoint 6 v6.15 |