Primary Device ID | B146ERW3GCN0 |
NIH Device Record Key | e14c9e30-4db2-4edc-b62c-50a6a2ed9e48 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ER9W wEvent 3GSM |
Version Model Number | 900-0614-01 |
Company DUNS | 049529118 |
Company Name | BRAEMAR MANUFACTURING, LLC |
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 | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
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 |
---|---|
HIBCC | B146ERW3GCN0 [Primary] |
DRG | Transmitters And Receivers, Physiological Signal, Radiofrequency |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-10-21 |
Device Publish Date | 2019-10-08 |
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