Primary Device ID | 00840682110693 |
NIH Device Record Key | b5e17e6a-3beb-44c0-88d8-0b35e5677845 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DISCOVERY |
Version Model Number | IGS 740 002 |
Company DUNS | 266062561 |
Company Name | GE MEDICAL SYSTEMS |
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 | 00840682110693 [Primary] |
JAA | System, x-ray, fluoroscopic, image-intensified |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-08-01 |
00840682125888 | IGS 7 OR 001 |
00840682124638 | IGS 7 001 |
00840682110693 | IGS 740 002 |
00840682110648 | IGS 730 002 |
00840682104739 | IGS 730 001 |