Primary Device ID | 10850689007824 |
NIH Device Record Key | 79d7e364-5249-4c77-83ce-49226443f210 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Dex Trodes |
Version Model Number | 202-277 |
Company DUNS | 080930531 |
Company Name | Compass Richmar, LLC |
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 | 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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10850689007824 [Primary] |
GXY | Electrode, Cutaneous |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2021-02-19 |
Device Publish Date | 2016-11-18 |
00850689007841 | 1.25" Round Foam |
00850689007834 | 3"x 5" Foam |
00850689007827 | 2" Round Foam |
00850689007810 | 2"x 3.5" Foam |
00850689007803 | 2"x 3.5" Cloth |
00850689007797 | 2" Round Cloth |
20850689007791 | 2"x 3.5" Cloth, Case of 10 |
10850689007848 | 1.25" Round Foam, Case of 10 |
10850689007831 | 3"x 5" Foam, Case of 10 |
10850689007824 | 2" Round Foam, Case of 10 |
10850689007817 | 2"x 3.5" Foam, Case of 10 |
10850689007794 | 2" Round Cloth, Case of 10 |