Duns Number:339182263
Device Description: Patient-interface for EEG ambulatory recorder
Catalog Number
-
Brand Name
BE Micro 21 CH MONO PLUG-IN HEADBOX
Version/Model Number
B8830073310
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)
-
Device labeled as "Not made with natural rubber latex"
-
For Single-Use
-
Prescription Use (Rx)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K093728
Product Code
GWL
Product Code Name
Amplifier, Physiological Signal
Public Device Record Key
5979dbe4-31c5-4d72-84cd-cabd1c948db8
Public Version Date
November 08, 2019
Public Version Number
2
DI Record Publish Date
April 02, 2019
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 67 |