Duns Number:007941230
Device Description: Mask Surgical Face PRIMASOFT160 For Sensitive Skin Anti-Fog Foam Anti Glare Strip With Ant Mask Surgical Face PRIMASOFT160 For Sensitive Skin Anti-Fog Foam Anti Glare Strip With Anti Glare Visor Tie Aluminum Nose Piece White Not Made With Natural Rubber Latex MediChoice
Catalog Number
-
Brand Name
Medichoice
Version/Model Number
PG4-5033
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)
-
Over the Counter (OTC)
-
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
c0ab02b4-9d8a-4725-acf6-488a2fde8adb
Public Version Date
July 07, 2020
Public Version Number
5
DI Record Publish Date
August 20, 2016
Package DI Number
50885632100732
Quantity per Package
4
Contains DI Package
10885632100734
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 428 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 8754 |
| U | Unclassified | 1 |