Primary Device ID | 00085971800729 |
NIH Device Record Key | 711f9d0c-46e1-44f8-b90e-7fcf9d881a8f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Hypoallergenic Electrode 2x2 4pk |
Version Model Number | BF5050 |
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 | true |
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 | 00085971800729 [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 | 2024-08-26 |
Device Publish Date | 2024-08-18 |
00085971800729 - Hypoallergenic Electrode 2x2 4pk | 2024-08-26 |
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