Duns Number:062388929
Device Description: Earloop Procedure Mask, blue, contains forming nosepiece, free of metal components, MRI co Earloop Procedure Mask, blue, contains forming nosepiece, free of metal components, MRI compatible, ASTM F2100 Level 2
Catalog Number
5303
Brand Name
Strong Manufacturers
Version/Model Number
5303
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Safe
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)
-
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
c7fee1ae-5d37-4d23-9705-43778b268f70
Public Version Date
February 03, 2022
Public Version Number
2
DI Record Publish Date
November 25, 2020
Package DI Number
10850005354366
Quantity per Package
300
Contains DI Package
00850005354369
Package Discontinue Date
February 02, 2022
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 | 79 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 5 |