Duns Number:966215829
Device Description: Duct Occluder II
Catalog Number
9-PDA2-03-04
Brand Name
Amplatzer™
Version/Model Number
Duct Occluder II
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"
Yes
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
MAE
Product Code Name
OCCLUDER, PATENT DUCTUS, ARTERIOSUS
Public Device Record Key
2ebe7310-7a5d-43ee-8800-257e3b86d9b8
Public Version Date
April 08, 2022
Public Version Number
6
DI Record Publish Date
September 08, 2014
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 1 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 63 |
| 3 | A medical device with high risk that requires premarket approval | 82 |