Duns Number:316153956
Device Description: Paired Subdermal Electrode YE, 12x2.5mm
Catalog Number
5140-534-624
Brand Name
NA
Version/Model Number
5140-534-624
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
Yes
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
-
Product Code
GWF
Product Code Name
STIMULATOR, ELECTRICAL, EVOKED RESPONSE
Public Device Record Key
8fe8758d-ec0b-4af0-b1ca-0efa9b0f245c
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
December 23, 2016
Package DI Number
37613327298117
Quantity per Package
10
Contains DI Package
07613327298116
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
pack
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 777 |
2 | A medical device with a moderate to high risk that requires special controls. | 2520 |