Primary Device ID | 05060441915139 |
NIH Device Record Key | 8d4871ee-fb8f-4e61-ac43-94c44277462b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GE Healthcare |
Version Model Number | 2104775-001 |
Catalog Number | 4010964C |
Company DUNS | 002111896 |
Company Name | GRAPHIC CONTROLS ACQUISITION CORP |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
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 | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | 800-669-6905 |
info@vermed.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05060441915139 [Primary] |
DSF | Recorder, Paper Chart |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-04-27 |
Device Publish Date | 2018-03-27 |
15060441915150 | Electrocardiographic recording paper |
05060441915139 | Electrocardiographic recording paper |
50009336009201 | Electrode |
50009336009195 | Electrode |
50009336009188 | Electrode |
50009336009171 | Electrode |
50009336009164 | Electrode |
50009336009157 | Electrode |
50009336009140 | Electrode |
50009336009133 | Electrode |
50009336009126 | electrodes |
50009336009119 | electrode |
50009336009102 | electrode |
50009336009096 | electrode |
50009336009089 | electrode |
50009336009072 | electrode |
50009336009065 | electrode |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
GE HEALTHCARE 97537319 not registered Live/Pending |
General Electric Company 2022-08-05 |
GE HEALTHCARE 97536608 not registered Live/Pending |
General Electric Company 2022-08-05 |