| Primary Device ID | 09005531002265 |
| NIH Device Record Key | cfd1d2a1-8926-4096-b9b6-8ab2bdfeef6c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Midmark |
| Version Model Number | RT41 |
| Catalog Number | 2-100-0207 |
| Company DUNS | 302846407 |
| Company Name | Leonhard Lang GmbH |
| Device Count | 100 |
| 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 | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Storage Environment Temperature | Between 5 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 30 Degrees Celsius |
| Storage Environment Temperature | Between 5 Degrees Celsius and 30 Degrees Celsius |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 09005531002265 [Unit of Use] |
| GS1 | 19005531002262 [Primary] |
| GS1 | 29005531002269 [Package] Contains: 19005531002262 Package: box [1000 Units] Discontinued: 2021-09-16 Not in Commercial Distribution |
| GS1 | 39005531002266 [Package] Contains: 29005531002269 Package: case [4000 Units] Discontinued: 2021-09-16 Not in Commercial Distribution |
| DRX | Electrode, Electrocardiograph |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-09-24 |
| Device Publish Date | 2021-09-16 |
| 29005531000159 - Skintact | 2025-08-01 ECG Electrode |
| 20869956000014 - S&W | 2025-04-04 Multifunction electrode for defibrillation, pacing, cardioversion, and monitoring |
| 30869956000028 - S&W | 2025-04-04 Multifunction electrode for defibrillation, pacing, cardioversion, and monitoring |
| 30869956000035 - S&W | 2025-04-04 Multifunction electrode for defibrillation, pacing, cardioversion, and monitoring |
| 30869956000042 - S&W | 2025-04-04 Multifunction electrode for defibrillation, pacing, cardioversion, and monitoring |
| 30869956000059 - S&W | 2025-04-04 Multifunction electrode for defibrillation, pacing, cardioversion, and monitoring |
| 30869956000066 - S&W | 2025-04-04 Multifunction electrode for defibrillation, pacing, cardioversion, and monitoring |
| 29005531000142 - SKINTACT | 2024-08-01 ECG Electrode |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MIDMARK 85375179 4321610 Live/Registered |
Midmark Corporation 2011-07-19 |
![]() MIDMARK 78284415 3294579 Live/Registered |
Midmark Corporation 2003-08-07 |
![]() MIDMARK 78262315 2978931 Dead/Cancelled |
Midmark Corporation 2003-06-13 |
![]() MIDMARK 75667102 2340810 Live/Registered |
MIDMARK INVESTMENTS, INC. 1999-03-24 |
![]() MIDMARK 75667075 2329255 Live/Registered |
MIDMARK INVESTMENTS, INC. 1999-03-24 |
![]() MIDMARK 73609374 1429861 Dead/Cancelled |
MIDMARK CORPORATION 1986-07-14 |
![]() MIDMARK 73171975 1150217 Live/Registered |
Midmark Corporation 1978-05-26 |
![]() MIDMARK 72455651 0986886 Dead/Cancelled |
I.E. INDUSTRIES, INC. 1973-04-26 |