Duns Number:806136177
Catalog Number
P154
Brand Name
PALMAZ Balloon Expandable Stent
Version/Model Number
P154
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Conditional
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
P890017,P890017
Product Code
MAF
Product Code Name
STENT, CORONARY
Public Device Record Key
63aad9e2-9bdc-402c-a443-d3f4813d0a25
Public Version Date
April 08, 2022
Public Version Number
6
DI Record Publish Date
May 07, 2015
Package DI Number
20705032057247
Quantity per Package
4
Contains DI Package
10705032076234
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 2567 |
3 | A medical device with high risk that requires premarket approval | 204 |