Duns Number:079226220
Device Description: CELL-DYN 22 Plus Control
Catalog Number
09H7201
Brand Name
CELL-DYN
Version/Model Number
09H72-01
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
-
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
K111211
Product Code
GLQ
Product Code Name
MIXTURE, CONTROL, WHITE-CELL AND RED-CELL INDICES
Public Device Record Key
423072a6-3e4d-4ffd-bebe-b458637be094
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
September 09, 2016
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 | 259 |
2 | A medical device with a moderate to high risk that requires special controls. | 245 |
U | Unclassified | 5 |