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 |
29005531000142 - SKINTACT | 2024-08-01 ECG Electrode |
29005531001125 - SKINTACT | 2024-08-01 ECG Electrode |
29005531000432 - SKINTACT | 2024-04-25 Pre-wired ECG Electrode |
29005531002535 - GE Healthcare | 2023-09-22 ECG Electrode |
29005531002542 - GE Healthcare | 2023-09-22 ECG Electrode |
29005531002559 - GE Healthcare | 2023-09-22 Pre-wired ECG Electrode |
29005531002566 - GE Healthcare | 2023-09-22 ECG Electrode |
29005531002573 - GE Healthcare | 2023-09-22 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 |