Duns Number:006261481
Device Description: MOTOR 95120-005 BIOCONSOLE 3L 540T EDM
Catalog Number
-
Brand Name
NA
Version/Model Number
95120-005
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
November 30, 2017
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
-
Prescription Use (Rx)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K941921
Product Code
DWA
Product Code Name
Control, pump speed, cardiopulmonary bypass
Public Device Record Key
fa1c6aa4-08d7-4a7c-8e6a-aabf16ef7728
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
June 18, 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 |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 102 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 20495 |
| 3 | A medical device with high risk that requires premarket approval | 3601 |