Duns Number:080935429
Device Description: Specialty Stimulating Electrodes
Catalog Number
PC90060
Brand Name
Uni-Patch
Version/Model Number
PC90060
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
February 17, 2021
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
-
Product Code
GXY
Product Code Name
ELECTRODE, CUTANEOUS
Public Device Record Key
7113af0c-0525-47ba-b233-c98de88158f2
Public Version Date
February 19, 2021
Public Version Number
9
DI Record Publish Date
September 24, 2016
Package DI Number
90884521168295
Quantity per Package
1000
Contains DI Package
10884521168299
Package Discontinue Date
February 17, 2021
Package Status
Not in Commercial Distribution
Package Type
CASE
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 672 |
2 | A medical device with a moderate to high risk that requires special controls. | 1692 |
U | Unclassified | 17 |