Primary Device ID | 10850958007463 |
NIH Device Record Key | d34e2680-bd35-43ec-afbc-eff8139428f3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sure Fit |
Version Model Number | 203-365 |
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 | 10850958007463 [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 |
00850958007466 | 2"x3.5" Cloth |
00850958007459 | 3"x5" Cloth |
00850958007442 | 2"x2" Cloth |
10850958007463 | 2"x3.5" Cloth, Case of 10 |
10850958007456 | 3"x5" Cloth, Case of 10 |
10850958007449 | 2"x2" Cloth, Case of 10 |