Primary Device ID | 00858688006971 |
NIH Device Record Key | 2b382a07-fdfa-4ec6-8a8d-5bcf14ef1b2e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Electrode 1.75 x 1.75 4 pack |
Version Model Number | ELEC0008B |
Company DUNS | 932471881 |
Company Name | Emsi |
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 | 00858688006971 [Primary] |
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 | 2023-09-28 |
Device Publish Date | 2023-09-20 |
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