Primary Device ID | B146PE31 |
NIH Device Record Key | bb20703d-e261-48a8-aa36-1b265746cbb2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Universal electrode patch |
Version Model Number | 02-01909 |
Company DUNS | 049529118 |
Company Name | BRAEMAR MANUFACTURING, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B146PE30 [Primary] |
HIBCC | B146PE31 [Package] Contains: B146PE30 Package: Box [40 Units] In Commercial Distribution |
DRX | Electrode, Electrocardiograph |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-03-29 |
Device Publish Date | 2022-03-21 |
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