Duns Number:968903703
Device Description: PS ASC-018-135 TRAILBLAZER ANGLED V03
Catalog Number
-
Brand Name
TrailBlazer™ Angled
Version/Model Number
ASC-018-135
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
K162384,K162384
Product Code
DQY
Product Code Name
Catheter, percutaneous
Public Device Record Key
fbbc23d0-6bb9-43b6-82e1-2ceaeeba9376
Public Version Date
December 22, 2021
Public Version Number
5
DI Record Publish Date
September 07, 2018
Package DI Number
20763000104683
Quantity per Package
5
Contains DI Package
00763000104689
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
PK
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 132 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 8540 |
| 3 | A medical device with high risk that requires premarket approval | 202 |
| U | Unclassified | 40 |