Duns Number:001660786
Device Description: BEQ-RF32 RotaFlow
Catalog Number
701049506
Brand Name
Descending Thoracic Pack
Version/Model Number
BEQ-T 22800
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
February 21, 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"
Yes
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
DWE
Product Code Name
Tubing, Pump, Cardiopulmonary Bypass
Public Device Record Key
dead5ccc-e5d1-45b9-b0f1-1300cc82262b
Public Version Date
February 21, 2019
Public Version Number
3
DI Record Publish Date
May 23, 2018
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 |