Duns Number:303639066
Device Description: VACUETTE® VISIO PLUS Needle 22G x 1" black, sterile, not made with natural rubber latex 0. VACUETTE® VISIO PLUS Needle 22G x 1" black, sterile, not made with natural rubber latex 0.7 x 25 mm
Catalog Number
450043
Brand Name
Vacuette
Version/Model Number
450043
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"
Yes
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
K061483,K061483,K061483,K061483
Product Code
FMI
Product Code Name
Needle, hypodermic, single lumen
Public Device Record Key
69293507-002a-4cbe-8e3b-866578f86fc0
Public Version Date
April 07, 2021
Public Version Number
5
DI Record Publish Date
September 23, 2016
Package DI Number
49120017570088
Quantity per Package
3
Contains DI Package
39120017570081
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 |