Primary Device ID | 00840682139359 |
NIH Device Record Key | 0a6d3033-38a9-4eb4-bd18-c69f2fd820b9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Discovery |
Version Model Number | 670 DR |
Company DUNS | 532102365 |
Company Name | G E MEDICAL SYSTEMS ISRAEL LTD. |
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 | false |
Serial Number | true |
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 | 00840682139359 [Primary] |
KPS | System, tomography, computed, emission |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2018-05-15 |
00840682139403 | NMCT 670 ES |
00840682139380 | NMCT 670 CZT |
00840682139373 | NMCT 670 PRO |
00840682139359 | 670 DR |
00840682139274 | NM 630 |
00840682124393 | 670 DR |
00840682123877 | NMCT 670 ES |
00840682123853 | NMCT 670 CZT |