Duns Number:557223252
Device Description: Hct Check - Low Level
Catalog Number
00009832350
Brand Name
Hct Check - Low Level
Version/Model Number
00009832350
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
March 09, 2018
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
-
Product Code
GLK
Product Code Name
CONTROL, HEMATOCRIT
Public Device Record Key
e7e2998f-cf37-4111-91d1-b48f72291fb7
Public Version Date
July 13, 2021
Public Version Number
5
DI Record Publish Date
September 23, 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 | 18 |
2 | A medical device with a moderate to high risk that requires special controls. | 272 |