Duns Number:092673953
Device Description: Mask, Pediatric, Non-Rebreather
Catalog Number
-
Brand Name
Mask, Pediatric, Non-Rebreather
Version/Model Number
3226-E
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
-
Product Code
KGB
Product Code Name
Mask, Oxygen, Non-Rebreathing
Public Device Record Key
5cc82960-effd-4b98-9844-c4f96c777bfa
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
April 17, 2017
Package DI Number
10709078002936
Quantity per Package
50
Contains DI Package
00709078002939
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 | 746 |
2 | A medical device with a moderate to high risk that requires special controls. | 320 |