Duns Number:316403245
Device Description: Centrifuge Bucket / Tube Holder (set of 4 matched units)A device intended to compensate fo Centrifuge Bucket / Tube Holder (set of 4 matched units)A device intended to compensate for and enable the use of different size test tubes and bottles in a centrifuge rotor bucket or centrifuge tube holder. This is a reusable device.
Catalog Number
4895-4
Brand Name
Bucket
Version/Model Number
4895-4
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)
-
Over the Counter (OTC)
Yes
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
KSO
Product Code Name
Centrifuge, Blood-Bank For In Vitro Diagnostic Use
Public Device Record Key
09fb8336-1181-444e-bf90-62d44a137f77
Public Version Date
September 13, 2021
Public Version Number
1
DI Record Publish Date
September 03, 2021
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 | 201 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 38 |