Duns Number:595138793
Device Description: Catheter 6FR, Percutaneous Sheath Introducer with Sideport Haemostasiss Valve OD 2.76mm x Catheter 6FR, Percutaneous Sheath Introducer with Sideport Haemostasiss Valve OD 2.76mm x ID 1.90mm, guidewire 0.9x450mm, introducer 1.4x70mm and stopcock.
Catalog Number
680122
Brand Name
SHEATH INTRO POP KIT 6FR L5 MULT=5/50
Version/Model Number
680122
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
-
Product Code
DYB
Product Code Name
Introducer, Catheter
Public Device Record Key
6cf98c31-01e8-488b-889d-8d8af30ba0db
Public Version Date
March 05, 2020
Public Version Number
3
DI Record Publish Date
September 22, 2016
Package DI Number
50886333601221
Quantity per Package
50
Contains DI Package
00886333601226
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
tyvek tray
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 2 | A medical device with a moderate to high risk that requires special controls. | 392 |