Primary Device ID | B14360200511 |
NIH Device Record Key | a84b1def-b1af-48cc-851c-39ad4d3a507e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SleepScout |
Version Model Number | Optional Sensor Kit |
Catalog Number | 602-0051 |
Company DUNS | 557510625 |
Company Name | Cleveland Medical Devices Inc. |
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 | true |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
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 | B14360200511 [Primary] |
GWQ | Full-Montage Standard Electroencephalograph |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-23 |
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B14360200511 | Optional accessory kit for use with SleepScout |
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B143502014610 | Wireless portable sleep monitor for sleep testing |
B14350101320 | Sapphire Computer Unit for recording/viewing Sapphire acquisition data in real time on a PC. |
B14350100280 | SPO2 Interface cable for use with SleepScout PSG system |