Duns Number:849234661
Device Description: EZ Scan Pack
Catalog Number
601003
Brand Name
E-Z-SCAN Low Viscosity UltraSound Gel
Version/Model Number
601003
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)
-
Over the Counter (OTC)
Yes
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
MUI
Product Code Name
Media,Coupling,Ultrasound
Public Device Record Key
0ad88665-a5f0-4d72-8bd3-74e712e3759a
Public Version Date
June 10, 2022
Public Version Number
3
DI Record Publish Date
September 23, 2016
Package DI Number
30815112020553
Quantity per Package
4
Contains DI Package
10815112020559
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Box
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 1 |
2 | A medical device with a moderate to high risk that requires special controls. | 28 |