Duns Number:711789789
Catalog Number
-
Brand Name
CANNULA
Version/Model Number
PR-24Q-1
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
August 12, 2022
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"
Yes
For Single-Use
-
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
K950729,K950729
Product Code
ODD
Product Code Name
Endoscopic retrograde cholangiopancreatography (ERCP) cannula
Public Device Record Key
4590083a-618d-4367-b20c-7af6e52b6405
Public Version Date
August 15, 2022
Public Version Number
7
DI Record Publish Date
September 21, 2016
Package DI Number
14953170043571
Quantity per Package
1
Contains DI Package
04953170043574
Package Discontinue Date
August 12, 2022
Package Status
Not in Commercial Distribution
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 117 |
2 | A medical device with a moderate to high risk that requires special controls. | 1962 |
U | Unclassified | 52 |