Duns Number:101835833
Device Description: Peel-away introducer set, 7F
Catalog Number
DYNJINTROPL7
Brand Name
Peel-away introducer set
Version/Model Number
DYNJINTROPL7
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
July 30, 2019
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
K073100,K073100
Product Code
DYB
Product Code Name
INTRODUCER, CATHETER
Public Device Record Key
4e979208-3524-4845-bb50-0a45be46147f
Public Version Date
September 13, 2021
Public Version Number
5
DI Record Publish Date
November 30, 2017
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 |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 592 |
3 | A medical device with high risk that requires premarket approval | 16 |