Duns Number:006999858
Device Description: COMPEL SINGLE WRAP KAUM 24X24 - RM (98 8282) USE: 27666202
Catalog Number
276U6602
Brand Name
ComPel Single Wrap
Version/Model Number
276U6602
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
-
Prescription Use (Rx)
-
Over the Counter (OTC)
Yes
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K923408,K923408
Product Code
FRG
Product Code Name
Wrap, Sterilization
Public Device Record Key
e3baf37b-5ee9-4d9d-b7eb-1501ba2e36d2
Public Version Date
November 08, 2019
Public Version Number
4
DI Record Publish Date
January 29, 2018
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 26 |
2 | A medical device with a moderate to high risk that requires special controls. | 9 |