Duns Number:014464314
Catalog Number
60050C
Brand Name
C-Core 60050C Laparotomy Pack VI-
Version/Model Number
60050C
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)
Yes
Device labeled as "Not made with natural rubber latex"
-
For Single-Use
Yes
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
K101598,K101598
Product Code
KKX
Product Code Name
Drape, Surgical
Public Device Record Key
8d5ea8da-6d75-471a-ad1f-bcb08757a855
Public Version Date
December 22, 2021
Public Version Number
6
DI Record Publish Date
September 27, 2016
Package DI Number
00817602022572
Quantity per Package
8
Contains DI Package
00817602022565
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Case
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 3 |
2 | A medical device with a moderate to high risk that requires special controls. | 489 |