Duns Number:044606982
Device Description: Colorectal Open Left Hemicolectomy/LAR Kit
Catalog Number
CRX21
Brand Name
N/A
Version/Model Number
CRX21
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
-
Product Code Name
-
Public Device Record Key
d3fff956-b0d7-4d96-b8b1-70655e53a1c9
Public Version Date
June 17, 2022
Public Version Number
6
DI Record Publish Date
February 15, 2018
Package DI Number
20705036015908
Quantity per Package
4
Contains DI Package
10705036015901
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
BOX
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 6 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 27 |
| U | Unclassified | 6 |