Duns Number:098554157
Catalog Number
-
Brand Name
Cadwell Disposable Disc Electrode
Version/Model Number
302294-000-120
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"
Yes
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
K110289,K110289
Product Code
GXY
Product Code Name
ELECTRODE, CUTANEOUS
Public Device Record Key
2f50159e-3e06-4388-90e2-dddb1d798cdd
Public Version Date
February 14, 2019
Public Version Number
5
DI Record Publish Date
September 05, 2016
Package DI Number
10840067100926
Quantity per Package
48
Contains DI Package
00840067100929
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Box
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 290 |