Duns Number:690724240
Catalog Number
-
Brand Name
Super Sheath
Version/Model Number
(15-707B) BT70Z07PGW035
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
K141070,K141070
Product Code
DYB
Product Code Name
INTRODUCER, CATHETER
Public Device Record Key
0b54d04d-e4b3-4038-ac1d-325670ac7ca1
Public Version Date
February 26, 2021
Public Version Number
7
DI Record Publish Date
September 16, 2016
Package DI Number
14543527202791
Quantity per Package
1
Contains DI Package
04543527202794
Package Discontinue Date
December 11, 2020
Package Status
Not in Commercial Distribution
Package Type
Box
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. | 211 |