Duns Number:412925992
Device Description: HemoTrol® WB is an assayed quality control material for professional use to verify the per HemoTrol® WB is an assayed quality control material for professional use to verify the performance characteristics of the HemoCue® Hb 301 and the HemoCue® Hb 801 System. HemoTrol® WB is intended for the quantitative determination of hemoglobin.
Catalog Number
08718734960959
Brand Name
HemoTrol WB
Version/Model Number
Normal
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
K182744,K182744
Product Code
GGM
Product Code Name
Control, Hemoglobin
Public Device Record Key
d50907ab-08cb-4dab-8308-a04c6ae3b747
Public Version Date
March 26, 2019
Public Version Number
1
DI Record Publish Date
March 18, 2019
Package DI Number
08718734960959
Quantity per Package
2
Contains DI Package
08718734960980
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 | 21 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 15 |