Duns Number:688460539
Device Description: Pediatric Resting ECG Electrodes, Mild Adhesive
Catalog Number
-
Brand Name
CareFusion
Version/Model Number
2009101-103P
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
K040784,K040784,K040784
Product Code
DRX
Product Code Name
Electrode, Electrocardiograph
Public Device Record Key
7d7d7a1a-7cab-4b69-aace-c25d3a597cdc
Public Version Date
July 06, 2018
Public Version Number
2
DI Record Publish Date
May 10, 2018
Package DI Number
28809083941387
Quantity per Package
14000
Contains DI Package
18809083941380
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Carton Box
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 53 |