Duns Number:175899459
Device Description: Agilis™ NxT Steerable Introducer: Bi-Directional, Large Curl 50.0 mm, 71 cm, 8.5F ID; Dila Agilis™ NxT Steerable Introducer: Bi-Directional, Large Curl 50.0 mm, 71 cm, 8.5F ID; Dilator: 94 cm
Catalog Number
STJG408324
Brand Name
NA
Version/Model Number
STJG408324
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"
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
K152090
Product Code
PNE
Product Code Name
Reprocessed catheter introducer
Public Device Record Key
75d99cff-4169-4767-bc1f-4b6ee8e3d85b
Public Version Date
August 14, 2019
Public Version Number
5
DI Record Publish Date
September 22, 2016
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 | 2763 |
2 | A medical device with a moderate to high risk that requires special controls. | 1372 |
U | Unclassified | 20 |