Duns Number:795104769
Device Description: Blanket, Full Underbody, White
Catalog Number
1924-0001
Brand Name
Soft Air
Version/Model Number
A400
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
c08093f4-cee0-4a08-8cec-5d5955cbdf6d
Public Version Date
August 06, 2019
Public Version Number
4
DI Record Publish Date
March 15, 2017
Package DI Number
20615089191101
Quantity per Package
10
Contains DI Package
10615089191104
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 |