Primary Device ID | 00850689007513 |
NIH Device Record Key | 09a01e56-1773-4d9e-b314-2fdd0cd5985f |
Commercial Distribution Discontinuation | 2018-12-31 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Adhesive Electrodes |
Version Model Number | 202-674 |
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 | false |
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 | 00850689007513 [Primary] |
GXY | Electrode, Cutaneous |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-12-31 |
Device Publish Date | 2016-09-01 |
00850689007513 | 1.5"x 3.5" Cloth |
00850689007506 | 3" Round Cloth |
00850689007490 | 1.25" Round Cloth |
00850689007483 | 2"x 3.5" Cloth |
00850689007476 | 2" Round Cloth |
00850689007469 | 2"x 2" Cloth |
10850689007510 | 1.5"x 3.5" Cloth, Case of 10 |
10850689007503 | 3" Round Cloth, Case of 10 |
10850689007497 | 1.25" Round Cloth, Case of 10 |
10850689007480 | 2"x 3.5" Cloth, Case of 10 |
10850689007473 | 2" Round Cloth, Case of 10 |
10850689007466 | 2"x 2" Cloth, Case of 10 |