Duns Number:938289980
Device Description: A plastic device designed to join two or more tubes of a cardiopulmonary bypass system cir A plastic device designed to join two or more tubes of a cardiopulmonary bypass system circuit, typically to create an extension or shunt; it may also be used to connect ancillary disposable devices (e.g., temperature probe). It typically has a Y-shape or straight design and is profiled at its ends to create leak-proof connections. This is a single-use device.
Catalog Number
332023NS
Brand Name
CONNECTOR, 1/4" X 3/8" W/O PART LINE W/LUER
Version/Model Number
332023NS
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In HIBCC
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
KRI
Product Code Name
Accessory Equipment, Cardiopulmonary Bypass
Public Device Record Key
e119af9e-b0f0-4d20-ba6f-9ea49a071ea6
Public Version Date
March 10, 2022
Public Version Number
3
DI Record Publish Date
October 13, 2015
Package DI Number
B066332023NS5
Quantity per Package
1000
Contains DI Package
B066332023NS1
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CASE
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 2 | A medical device with a moderate to high risk that requires special controls. | 50 |