Duns Number:078330362
Device Description: Accessory for the CritiCool system. Abody wrap connected to the CritiCool.
Catalog Number
PED-M1001
Brand Name
CureWrap™
Version/Model Number
Medium1 Pediatric 7-11 kg (single)
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
4bf07afe-3964-4bb7-8311-95e28506fa7a
Public Version Date
September 09, 2021
Public Version Number
3
DI Record Publish Date
September 24, 2016
Package DI Number
77290107580143
Quantity per Package
4
Contains DI Package
07290107580144
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Box
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 163 |