| Primary Device ID | 50009336009065 | 
| NIH Device Record Key | 987dcaaa-e20b-4bef-81f7-2e451ec643e1 | 
| Commercial Distribution Discontinuation | 2021-10-11 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | GE Healthcare | 
| Version Model Number | 2104777-001 | 
| Catalog Number | 32029050 | 
| Company DUNS | 002111896 | 
| Company Name | GRAPHIC CONTROLS ACQUISITION CORP | 
| Device Count | 60 | 
| DM Exempt | false | 
| Pre-market Exempt | true | 
| MRI Safety Status | MR Conditional | 
| 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 | true | 
| Donation Id Number | false | 
| Contains Natural Rubber Latex | false | 
| Labeled No Natural Rubber Latex | true | 
| RX Perscription | true | 
| OTC Over-The-Counter | false | 
| Phone | 1.800.669.6905 | 
| customerservice@vermed.com | |
| Phone | 1.800.669.6905 | 
| customerservice@vermed.com | |
| Phone | 1.800.669.6905 | 
| customerservice@vermed.com | |
| Phone | 1.800.669.6905 | 
| customerservice@vermed.com | |
| Phone | 1.800.669.6905 | 
| customerservice@vermed.com | |
| Phone | 1.800.669.6905 | 
| customerservice@vermed.com | |
| Phone | 1.800.669.6905 | 
| customerservice@vermed.com | |
| Phone | 1.800.669.6905 | 
| customerservice@vermed.com | |
| Phone | 1.800.669.6905 | 
| customerservice@vermed.com | |
| Phone | 1.800.669.6905 | 
| customerservice@vermed.com | |
| Phone | 1.800.669.6905 | 
| customerservice@vermed.com | |
| Phone | 1.800.669.6905 | 
| customerservice@vermed.com | |
| Phone | 1.800.669.6905 | 
| customerservice@vermed.com | |
| Phone | 1.800.669.6905 | 
| customerservice@vermed.com | |
| Phone | 1.800.669.6905 | 
| customerservice@vermed.com | |
| Phone | 1.800.669.6905 | 
| customerservice@vermed.com | |
| Phone | 1.800.669.6905 | 
| customerservice@vermed.com | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00009336009060 [Unit of Use] | 
| GS1 | 10009336009067 [Primary] | 
| GS1 | 50009336009065 [Package] Contains: 10009336009067 Package: [600 Units] Discontinued: 2021-10-11 In Commercial Distribution  | 
| DRX | Electrode, Electrocardiograph | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 2 | 
| Public Version Date | 2020-03-31 | 
| Device Publish Date | 2018-04-12 | 
| 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  |