Duns Number:041810693
Catalog Number
9620
Brand Name
44 in (112 cm) CheckMate Extension set
Version/Model Number
9620
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
February 13, 2019
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
FPA
Product Code Name
Set, Administration, Intravascular
Public Device Record Key
d2d45e0a-1a05-4dce-bb8c-c1655a8cac5d
Public Version Date
June 11, 2019
Public Version Number
3
DI Record Publish Date
July 29, 2016
Package DI Number
20634624096206
Quantity per Package
50
Contains DI Package
00634624096202
Package Discontinue Date
February 13, 2019
Package Status
Not in Commercial Distribution
Package Type
Shiipper
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 22 |
2 | A medical device with a moderate to high risk that requires special controls. | 168 |
U | Unclassified | 8 |