Primary Device ID | 80092237622045 |
NIH Device Record Key | a477aa7a-e7bc-4e57-80f5-a2257b75fee3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Tens 7000 Conductive Sleeves |
Version Model Number | DT7202-SLEEVE |
Company DUNS | 827221698 |
Company Name | COMPASS HEALTH BRANDS CORP. |
Device Count | 2 |
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 | true |
RX Perscription | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00092237622049 [Primary] |
GS1 | 01092237622048 [Unit of Use] |
GS1 | 80092237622045 [Package] Contains: 00092237622049 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 | 2019-11-28 |
Device Publish Date | 2019-11-20 |
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