Duns Number:001660786
Device Description: HMO 70000 (BO coated) Quadrox i AdultBO-VHK 71000 Venous ReservoirBO-RF32 RotaFlowCDI Sat HMO 70000 (BO coated) Quadrox i AdultBO-VHK 71000 Venous ReservoirBO-RF32 RotaFlowCDI Sat Cell 1/2" System 100Prebypass filter w/o Vent Porous Media 3/8x1/2Gas Filter
Catalog Number
701067372
Brand Name
Open Heart without Plegiox
Version/Model Number
BO-TOP 14605
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
July 20, 2018
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)
Yes
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
DWF
Product Code Name
Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
Public Device Record Key
f96dc147-6951-43ca-83bd-0d2eac7dbea5
Public Version Date
January 28, 2019
Public Version Number
5
DI Record Publish Date
November 20, 2015
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. | 663 |