Duns Number:795104769
Device Description: Blanket, Tube, White
Catalog Number
1920-0001
Brand Name
Soft Air
Version/Model Number
A510
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
DWJ
Product Code Name
System, Thermal Regulating
Public Device Record Key
fb69f5b5-d2c4-4491-904c-72163316ed34
Public Version Date
August 06, 2019
Public Version Number
4
DI Record Publish Date
March 15, 2017
Package DI Number
20615089192009
Quantity per Package
10
Contains DI Package
10615089192002
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Carton
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 16 |
2 | A medical device with a moderate to high risk that requires special controls. | 93 |