Duns Number:442126587
Catalog Number
-
Brand Name
BRAT 2
Version/Model Number
BOWL PROCESSING SET - 135 ml
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
K974897,K974897
Product Code
CAC
Product Code Name
APPARATUS, AUTOTRANSFUSION
Public Device Record Key
de0c424e-92d1-4f7d-86c7-82f44d62ff95
Public Version Date
January 08, 2021
Public Version Number
4
DI Record Publish Date
July 06, 2015
Package DI Number
38033178106048
Quantity per Package
6
Contains DI Package
08033178106047
Package Discontinue Date
-
Package Status
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 | 25 |
2 | A medical device with a moderate to high risk that requires special controls. | 398 |
3 | A medical device with high risk that requires premarket approval | 78 |