Duns Number:303639066
Device Description: VACUETTE® SECONDARY Tube MULTIPLEX PP 13x75 mm with white screw closure, PREMIUM
Catalog Number
459000
Brand Name
Vacuette
Version/Model Number
459000
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
-
Product Code
NNI
Product Code Name
CONTAINER, SPECIMEN, NON-STERILE
Public Device Record Key
649c6594-15e9-4f3e-b3e0-1ccf28191296
Public Version Date
February 21, 2022
Public Version Number
2
DI Record Publish Date
September 24, 2020
Package DI Number
39120017578346
Quantity per Package
4
Contains DI Package
29120017578349
Package Discontinue Date
-
Package Status
In Commercial Distribution
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. | 21 |