Primary Device ID | 80092237900457 |
NIH Device Record Key | 918a7e08-bbde-4232-b125-be0917afbd07 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Medidcal Science Products Private Label |
Version Model Number | 203-483 |
Company DUNS | 080930531 |
Company Name | Compass Richmar, LLC |
Device Count | 4 |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00092237900451 [Primary] |
GS1 | 01092237900450 [Unit of Use] |
GS1 | 30092237900452 [Package] Contains: 00092237900451 Package: Inner Carton [10 Units] In Commercial Distribution |
GS1 | 80092237900457 [Package] Contains: 30092237900452 Package: Master carton [50 Units] In Commercial Distribution |
GXY | Electrode, Cutaneous |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-02-07 |
Device Publish Date | 2019-01-07 |
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