Duns Number:078474365
Device Description: Earloop Procedure Masks, ASTM Level 3, White, Box
Catalog Number
5722017
Brand Name
Edge™ EarLoop Procedure Masks
Version/Model Number
5722017
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)
-
Over the Counter (OTC)
Yes
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
FXX
Product Code Name
Mask, Surgical
Public Device Record Key
52c307b0-fdad-4e14-8e69-23a95fb9b4b8
Public Version Date
May 06, 2020
Public Version Number
2
DI Record Publish Date
February 06, 2020
Package DI Number
20818365020991
Quantity per Package
10
Contains DI Package
10818365020994
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Case
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 2 | A medical device with a moderate to high risk that requires special controls. | 25 |
| U | Unclassified | 3 |